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Dayang Chem (Hangzhou) Co.,Ltd.

Dayangchem's R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. DayangChem can provide different quantities

1-Bromo-4-nitrobenzene Manufacturer/High quality/Best price/In stock

Cas:586-78-7

Min.Order:1 Kilogram

FOB Price: $3.0

Type:Lab/Research institutions

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Hangzhou Dingyan Chem Co., Ltd

Items Standard Result Assay (Ursolic acid) 98%min 98.22% ----------------------------------------------------------------

High purity 586-78-7 1-Bromo-4-nitrobenzene

Cas:586-78-7

Min.Order:1 Gram

FOB Price: $100.0 / 500.0

Type:Trading Company

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Simagchem Corporation

Welcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our

High quality 1-bromo-4-nitrobenzene supplier in China

Cas:586-78-7

Min.Order:0 Metric Ton

Negotiable

Type:Manufacturers

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Henan Allgreen Chemical Co.,Ltd

high quality Appearance:Colorless liquid Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea Port:shanghai

1-bromo-4-nitrobenzene

Cas:586-78-7

Min.Order:1 Kilogram

Negotiable

Type:Manufacturers

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Chemwill Asia Co., Ltd.

Our main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block

4-Bromonitrobenzene

Cas:586-78-7

Min.Order:5 Kiloliter

FOB Price: $1.2 / 5.0

Type:Manufacturers

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Hebei yanxi chemical co.,LTD.

chengdu and import and export trade co., LTD., who registered capital of 10 million yuan, nearly to $2 million, we have a pharmaceutical raw materials factory production of pharmaceutical raw materials, and a reagent r&d center, and we do res

1-Bromo-4-nitrobenzene

Cas:586-78-7

Min.Order:5 Metric Ton

FOB Price: $1100.0 / 1500.0

Type:Trading Company

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Jinan Finer Chemical Co., Ltd

Product Description Name 1-Bromo-4-nitrobenzene CAS 586-78-7 Assay 99% Appearance

1-Bromo-4-nitrobenzene

Cas:586-78-7

Min.Order:1 Kilogram

Negotiable

Type:Lab/Research institutions

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Henan Tianfu Chemical Co., Ltd.

1-Bromo-4-nitrobenzene Basic information Product Name: 1-Bromo-4-nitrobenzene Synonyms: p-Nitrobromobenzene;P-BROMONITROBENZENE;4-BROMONITROBENZENE;4-bromo-1-nitrobenzene;4-NITROBROMOBEN

1-Bromo-4-nitrobenzene586-78-7

Cas:586-78-7

Min.Order:1 Metric Ton

Negotiable

Type:Lab/Research institutions

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Henan Sinotech Import&Export Corporation

Identification Product name: 1-bromo-4-nitrobenzene Product name: 1-bromo-4-nitrobenzene Molec

1-bromo-4-nitrobenzene

Cas:586-78-7

Min.Order:5 Metric Ton

FOB Price: $1.0 / 2.0

Type:Other

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Hangzhou Keyingchem Co.,Ltd

Hangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det

1-bromo-4-nitrobenze

Cas:586-78-7

Min.Order:0 Metric Ton

Negotiable

Type:Lab/Research institutions

inquiry

SHANGHAI T&W PHARMACEUTICAL CO., LTD.

A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc

1-Bromo-4-nitrobenzene

Cas:586-78-7

Min.Order:4 Kilogram

Negotiable

Type:Lab/Research institutions

inquiry

Hangzhou J&H Chemical Co., Ltd.

J&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia

1-Bromo-4-nitrobenzene

Cas:586-78-7

Min.Order:0

Negotiable

Type:Lab/Research institutions

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Zibo Hangyu Biotechnology Development Co., Ltd

Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi

High quality 1-bromo-4-nitrobenzene

Cas:586-78-7

Min.Order:10 Gram

FOB Price: $100.0

Type:Lab/Research institutions

inquiry

Henan Wentao Chemical Product Co., Ltd.

We are leading fine chemicals supplier in China with ISO certificate, Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED

1-Bromo-4-nitrobenzeneCAS NO.: 586-78-7

Cas:586-78-7

Min.Order:1 Gram

FOB Price: $2.0

Type:Lab/Research institutions

inquiry

Suzhou Sinosun Imp.&Exp. Corporation

We're in good position to supply OLED intermediates . In the past 25 years, we have won technical support from several well-known universities and institutes. We have developed many chemicals together. It makes us capable of developing Cust

1-bromo-4-nitrobenzene

Cas:586-78-7

Min.Order:100 Kilogram

Negotiable

Type:Trading Company

inquiry

Hangzhou Zhongqi chem Co.,Ltd.

Located in Hangzhou National Hi-Tech Industrial Development Zone, zhongqichem is a technical company mainly focus on the Custom synthesis, manufacturing, sales of chemicals to various industries. Benefiting from the outstanding customer service and h

1-Bromo-4-nitrobenzene

Cas:586-78-7

Min.Order:0

Negotiable

Type:Other

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Hunan chemfish Pharmaceutical co.,Ltd

Appearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea

1-Bromo-4-nitrobenzene

Cas:586-78-7

Min.Order:0

Negotiable

Type:Manufacturers

inquiry

Kono Chem Co.,Ltd

high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou

1-Bromo-4-nitrobenzene

Cas:586-78-7

Min.Order:0

Negotiable

Type:Other

inquiry

GIHI CHEMICALS CO.,LIMITED

high purity,in stock Package:25kg/drum,or as per customers'demand Application:API,or Intermediates,fine chemicals Transportation:air,sea,courier

p-Bromonitrobenzene

Cas:586-78-7

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

JINHUA HUAYI CHEMICAL CO., LTD.

Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands

1-Bromo-4-Nitrobenzene

Cas:586-78-7

Min.Order:100 Gram

Negotiable

Type:Lab/Research institutions

inquiry

HANGZHOU YUNUO CHEMICAL CO.,LTD

Superior quality, moderate price & quick delivery. Appearance:white crystalline powder Storage:Sealed in a cool ,dry and microtherm place , avoid light . Package:10kg/drum;200kg/drum as per your request Application:It is an important raw mater

1-Bromo-4-nitrobenzene supplier in China

Cas:586-78-7

Min.Order:10 Kilogram

Negotiable

Type:Trading Company

inquiry

Aecochem Corp.

Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS

1-bromo-4-nitrobenzene

Cas:586-78-7

Min.Order:0

Negotiable

Type:Manufacturers

inquiry

Enke Pharma-tech Co.,Ltd. (Cangzhou, China )

Cangzhou Enke Pharma Tech Co.,ltd. is located in Cangzhou City, Hebei province ,where is a famous petroleum chemical industry city?in China. Enke Pharma a high-tech enterprise ,and we are dedicated to developing and manufacturing new api,?intermediat

4-Bromonitrobenzene

Cas:586-78-7

Min.Order:0

Negotiable

Type:Manufacturers

inquiry

Antimex Chemical Limied

Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali

1-BroMo-4-nitrobenzene

Cas:586-78-7

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Xiamen AmoyChem Co.,Ltd

Amoychem is committed to providing the top-quality chemical products and services Internationally. We offer our customers with friendly, professional service and reliable, high performance products that have been manufactured according to the accredi

1-bromo-4-nitrobenzene

Cas:586-78-7

Min.Order:0

Negotiable

Type:Other

inquiry

Hangzhou JINLAN Pharm-Drugs Technology Co., Ltd

Name 1-Bromo-4-nitrobenzene Synonyms 4-Bromo-1-nitrobenzene Molecular Structure Molecular Formula

1-Bromo-4-nitrobenzene

Cas:586-78-7

Min.Order:0 Metric Ton

Negotiable

Type:Other

inquiry

Hubei Langyou International Trading Co., Ltd

TIANFUCHEM--High purity 1-Bromo-4-nitrobenzene factory price Application:TIANFUCHEM--High purity 1-Bromo-4-nitrobenzene factory price

TIANFUCHEM--High purity 1-Bromo-4-nitrobenzene factory price

Cas:586-78-7

Min.Order:0

Negotiable

Type:Other

inquiry

Hangzhou ZeErRui Chemical Co., Ltd.

Hangzhou ZeErRui Chemical Co., Ltd. located in Lingang industrial areas, our plant covers an area of 6000 square meters.ZeErRui dedicated to the development, production and marketing of chemicals. We have earned ourselves a good reputation at home an

1-Bromo-4-nitrobenzene manufacture

Cas:586-78-7

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Hunan Longxianng Runhui Trading Co.,Ltd

TIANFUCHEM--High purity 1-Bromo-4-nitrobenzene factory priceAppearance:powder Storage:room tempurature Package:As required Application:medical Transportation:By express (Door to door) such as FEDEX, DHL, EMS for small amount. By air(airport to airpor

TIANFUCHEM--High purity 1-Bromo-4-nitrobenzene factory price

Cas:586-78-7

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Hunan Russell Chemicals Technology Co.,Ltd

high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China

1-Bromo-4-nitrobenzene 586-78-7

Cas:586-78-7

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Synthetic route

4-nitrobenzenediazonium tetrafluoroborate
456-27-9

4-nitrobenzenediazonium tetrafluoroborate

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With dibenzo-18-crown-6; potassium bromide; copper(ll) bromide; 1,10-Phenanthroline; copper(I) bromide In acetonitrile at 20℃; for 0.333333h; Sandmeyer bromination;99%
With N-Bromosuccinimide; tetrabutylammonium perchlorate In methanol; N,N-dimethyl-formamide at 20℃; for 1h; Sandmeyer Reaction; Electrochemical reaction;84%
With 1,3-bis-n-butylimidazolium bromide at 80℃; for 0.5h;71%
4-Bromophenylboronic acid
5467-74-3

4-Bromophenylboronic acid

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With nitric acid In 1,2-dichloro-ethane at 70℃; for 16h; Inert atmosphere;98%
With copper(II) nitrate trihydrate; trifluoroacetic acid In ethyl acetate at 100℃; for 3h;96%
With 1,1,1,3',3',3'-hexafluoro-propanol; 2-nitrobenzo[d]isothiazol-3(2H)-one 1,1-dioxide at 60℃; for 19h; Reagent/catalyst; Inert atmosphere; Schlenk technique;96%
2-bromo-5-nitrobenzoic acid
943-14-6

2-bromo-5-nitrobenzoic acid

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With silver carbonate In dimethyl sulfoxide at 120℃; for 16h;97%
With silver carbonate In dimethyl sulfoxide at 120℃;
4-nitrophenylhydrazine hydrochloride
636-99-7

4-nitrophenylhydrazine hydrochloride

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With boron tribromide; dimethyl sulfoxide at 80℃; for 1h;97%
bis(4-bromophenyl)iodonium triflate
139139-81-4

bis(4-bromophenyl)iodonium triflate

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With sodium nitrite In ethyl acetate at 70℃; for 16h; Temperature; Solvent; Sealed tube; regioselective reaction;96%
4-bromo-aniline
106-40-1

4-bromo-aniline

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With 3-chloro-benzenecarboperoxoic acid In toluene for 3h; Reflux;95%
With tert.-butylhydroperoxide In acetonitrile at 60℃; for 4h; Reagent/catalyst; Temperature; Solvent; Schlenk technique;91%
With tert.-butylhydroperoxide; 3 A molecular sieve; zirconium(IV) tert-butoxide In dichloromethane for 1.5h; Ambient temperature;89%
1-bromo-2-naphthol
573-97-7

1-bromo-2-naphthol

4-nitrobenzenediazonium o-benzenedisulfonimide

4-nitrobenzenediazonium o-benzenedisulfonimide

A

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

B

para red
6410-10-2

para red

Conditions
ConditionsYield
With sodium hydroxide; tetraethylammonium bromide In acetonitrile at 20℃; for 10h; Product distribution; Further Variations:; Reagents; Reaction partners;A 80%
B 15%
4-nitrobenzenediazonium 4-methylbenzenesulfonate
1947-33-7

4-nitrobenzenediazonium 4-methylbenzenesulfonate

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With potassium bromide In water at 20℃; for 1h;80%
tert-butyl 2-(4-nitrophenyl)diazenecarboxylate
92722-14-0

tert-butyl 2-(4-nitrophenyl)diazenecarboxylate

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With Bromotrichloromethane; trifluoroacetic acid In benzene at 20℃;79%
With Bromotrichloromethane; trifluoroacetic acid In acetonitrile at 80℃; for 0.5h;57%
bromobenzene
108-86-1

bromobenzene

A

2-nitrophenyl bromide
577-19-5

2-nitrophenyl bromide

B

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With nitric acid at 50℃; for 3h;A 20.9%
B 78.2%
With Iron(III) nitrate nonahydrate; phosphorus pentoxide In neat (no solvent) at 20℃; for 6h; Milling; Green chemistry; Overall yield = 93 percent;A 25%
B 68%
With thionyl chloride; bismuth subnitrate In dichloromethane at 20℃; for 9h;A 18%
B 60%
4-bromo-N,N-dimethylaniline
586-77-6

4-bromo-N,N-dimethylaniline

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With tert.-butylhydroperoxide; ammonium iodide; water In dimethyl sulfoxide at 90℃; for 4h; Sealed tube;73%
p-nitrobenzene iodide
636-98-6

p-nitrobenzene iodide

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With nickel dibromide In N,N-dimethyl-formamide at 170℃; for 0.0833333h; microwave irradiation;72%
para-dinitrobenzene
100-25-4

para-dinitrobenzene

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
Stage #1: para-dinitrobenzene With perchloric acid; sulfuric acid; sodium nitrite In water; ethyl acetate Electrochemical reaction;
Stage #2: With hydrogen bromide; copper In water Electrochemical reaction;
67%
acrylonitrile
107-13-1

acrylonitrile

4-nitrophenylhydrazone
100-16-3

4-nitrophenylhydrazone

A

2-bromo-3-(4-nitro-phenyl)-propionitrile
62448-25-3

2-bromo-3-(4-nitro-phenyl)-propionitrile

B

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With copper(ll) bromide In water; acetic acid for 1h;A 30%
B 60%
With copper(II) sulfate; sodium bromide In water; acetic acid for 1h;A 48%
B 35%
4-nitro-benzoic acid
62-23-7

4-nitro-benzoic acid

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With [bis(acetoxy)iodo]benzene; bromine In various solvent(s) for 22h; bromodecarboxylation; Heating; irradiation;59%
With Bromotrichloromethane; 2,2’-disulfanediyldipyridine-1-oxide 2.) o-dichlorobenzene, 130 deg C; Yield given. Multistep reaction;
4-nitro-aniline
100-01-6

4-nitro-aniline

allyl bromide
106-95-6

allyl bromide

A

1-allyl-4-nitro-benzene
53483-17-3

1-allyl-4-nitro-benzene

B

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With tert.-butylnitrite In acetonitrile at 50℃; for 1.33h;A 55%
B n/a
C7H6N8O2
93680-31-0

C7H6N8O2

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With tetrabutylammomium bromide; trifluoroacetic acid In acetonitrile at 70 - 80℃;52%
acrylic acid methyl ester
292638-85-8

acrylic acid methyl ester

4-nitrophenylhydrazone
100-16-3

4-nitrophenylhydrazone

A

2-Bromo-3-(4-nitro-phenyl)-propionic acid methyl ester
126558-68-7

2-Bromo-3-(4-nitro-phenyl)-propionic acid methyl ester

B

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With copper(II) sulfate; sodium bromide In water; acetic acid for 1h;A 47%
B 42%
4-Bromophenylboronic acid
5467-74-3

4-Bromophenylboronic acid

A

2,4-dinitrobromobenzene
584-48-5

2,4-dinitrobromobenzene

B

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With ammonium nitrate; trifluoroacetic anhydride In acetonitrile at -35℃; for 5h; Nitration; Ipso-nitration;A 42%
B 37%
para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

4-bromo-aniline
106-40-1

4-bromo-aniline

Conditions
ConditionsYield
With copper(I) chloride; potassium borohydride In methanol for 0.166667h; Ambient temperature;100%
With sodium tetrahydroborate In methanol at 60℃; for 3h; Sealed tube;100%
With water; oxalic acid; titanium(IV) oxide for 3h; Wavelength; Irradiation; Inert atmosphere; Sealed tube; Green chemistry; chemoselective reaction;100%
pyrrolidine
123-75-1

pyrrolidine

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

1-(4-nitro-phenyl)-pyrrolidine
10220-22-1

1-(4-nitro-phenyl)-pyrrolidine

Conditions
ConditionsYield
In tetrahydrofuran at 50℃; under 6375510 Torr; for 20h;100%
In tetrahydrofuran at 50℃; under 9000720 Torr; for 20h;100%
With C30H25BrN3PPdS; potassium carbonate In iso-butanol at 100℃; for 24h; Buchwald-Hartwig Coupling; Inert atmosphere;99.4%
1,4-diaza-bicyclo[2.2.2]octane
280-57-9

1,4-diaza-bicyclo[2.2.2]octane

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

1-(4-Nitro-phenyl)-4-aza-1-azonia-bicyclo[2.2.2]octane; bromide
112473-27-5

1-(4-Nitro-phenyl)-4-aza-1-azonia-bicyclo[2.2.2]octane; bromide

Conditions
ConditionsYield
In tetrahydrofuran at 50℃; under 4500360 Torr; for 75h;100%
In tetrahydrofuran at 50℃; under 4500360 Torr; for 20h; Yield given;
phenylacetylene
536-74-3

phenylacetylene

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

4-(phenylethynyl)nitrobenzene
1942-30-9

4-(phenylethynyl)nitrobenzene

Conditions
ConditionsYield
With potassium carbonate In ethanol; water at 65℃; for 8h; Sonogashira Cross-Coupling; Inert atmosphere;100%
With 1,4-diaza-bicyclo[2.2.2]octane; PdCl2[4,4'-bis(n-C10F21CH2OCH2)-2,2'-bipyridine] In N,N-dimethyl-formamide at 140℃; for 0.5h; Catalytic behavior; Sonogashira Cross-Coupling; Microwave irradiation;100%
With copper(l) iodide; triethylamine; triphenylphosphine In water at 60℃; for 24h; Catalytic behavior; Solvent; Reagent/catalyst; Temperature; Time; Sonogashira Cross-Coupling; Schlenk technique; Inert atmosphere;100%
para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

phenol
108-95-2

phenol

4-nitrophenyl phenyl ether
620-88-2

4-nitrophenyl phenyl ether

Conditions
ConditionsYield
With caesium carbonate; copper(I) bromide; 1,1'-azobis(1-cyanocyclohexanenitrile) In N,N-dimethyl-formamide at 100℃; for 1.5h; Reagent/catalyst; Temperature; Solvent; Microwave irradiation; Green chemistry;100%
With potassium fluoride; copper(II) ion; silica gel In dimethyl sulfoxide at 130℃; for 16h; Ullmann diaryl etherification;98%
With caesium carbonate; potassium iodide In N,N-dimethyl-formamide at 120℃; for 22h; Ullmann condensation; Inert atmosphere;95%
para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

phenylboronic acid
98-80-6

phenylboronic acid

1-phenyl-4-nitrobenzene
92-93-3

1-phenyl-4-nitrobenzene

Conditions
ConditionsYield
With sodium carbonate; palladium on activated charcoal In ethanol at 20℃; for 2h; Suzuki-Miyaura cross-coupling;100%
With PdCl*(2-({[(2-methylselanyl)ethyl]imino}methyl)benzenol); potassium carbonate In N,N-dimethyl-formamide at 100℃; for 24h; Suzuki-Miyaura cross-coupling;100%
With 1,4-diaza-bicyclo[2.2.2]octane; caesium carbonate; palladium diacetate In N,N-dimethyl-formamide at 40℃; for 16h; Suzuki-Miyaura cross-coupling;100%
para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

β-naphthol
135-19-3

β-naphthol

4-nitrophenyl 2-naphthyl ether
71311-82-5

4-nitrophenyl 2-naphthyl ether

Conditions
ConditionsYield
With caesium carbonate; copper(I) bromide; 1,1'-azobis(1-cyanocyclohexanenitrile) In N,N-dimethyl-formamide at 100℃; for 0.5h; Microwave irradiation; Green chemistry;100%
With copper(l) iodide; 2-carbomethoxy-3-hydroxyquinoxaline-di-N-oxide; caesium carbonate In N,N-dimethyl-formamide at 100℃; for 12h; Schlenk technique; Inert atmosphere;93%
With potassium carbonate In dimethyl sulfoxide at 80℃; for 12h; Catalytic behavior; Ullmann Condensation; Sealed tube; Schlenk technique;91%
2-methyl-but-3-yn-2-ol
115-19-5

2-methyl-but-3-yn-2-ol

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

2-methyl-4-(4-nitrophenyl)but-3-yn-2-ol
33432-53-0

2-methyl-4-(4-nitrophenyl)but-3-yn-2-ol

Conditions
ConditionsYield
With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine In tetrahydrofuran for 12h; Sonogashira Cross-Coupling; Inert atmosphere; Reflux;100%
With copper(l) iodide; triethylamine; triphenylphosphine at 90℃; for 3h; Sonogashira coupling; Inert atmosphere;97%
With copper(l) iodide; triethylamine; bis-triphenylphosphine-palladium(II) chloride In tetrahydrofuran for 12h; Heating;96%
styrene
292638-84-7

styrene

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

trans-4-nitrostilbene
1694-20-8

trans-4-nitrostilbene

Conditions
ConditionsYield
With tetramethylquanidine; sodium acetate; palladium dichloride In N,N-dimethyl acetamide at 140℃; for 20h; Heck reaction;100%
With 2-n-butyl-1,1,1,3,3-tetramethylguanidine acetate; palladium dichloride at 140℃; for 0.25h;99%
With 0.42C23H20N4O4*2Cl(1-)*Zn(2+)*10.16H2O*0.58Pd(2+)*0.58C23H20N4O4(1-); potassium carbonate In N,N-dimethyl acetamide at 100℃; for 1h; Heck Reaction;99%
acrylic acid n-butyl ester
141-32-2

acrylic acid n-butyl ester

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

(E)-n-butyl 4-nitrocinnamate
86622-84-6, 131061-15-9

(E)-n-butyl 4-nitrocinnamate

Conditions
ConditionsYield
With tetramethylquanidine; sodium acetate; palladium dichloride In N,N-dimethyl acetamide at 140℃; for 20h; Heck reaction;100%
With 2-n-butyl-1,1,1,3,3-tetramethylguanidine acetate; palladium dichloride at 140℃; for 0.25h;100%
With tri-n-propylamine In 1-methyl-pyrrolidin-2-one at 125℃; for 1h; Mizoroki-Heck reaction; Inert atmosphere;100%
para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

ethyl acrylate
140-88-5

ethyl acrylate

ethyl (E)-3-(4-nitrophenyl)-2-propenoate
24393-61-1

ethyl (E)-3-(4-nitrophenyl)-2-propenoate

Conditions
ConditionsYield
With triethylamine; {[Pd(η5-C5H5)Fe(η5-C5H3)C(CH3)=N(C6H4CH3-4)](μ-I)}2 In 1,4-dioxane at 100℃; for 10h;100%
With potassium phosphate; tetrabutylammomium bromide; [PdCl{[η5-C5H5)]Fe[(η5-C5H3)C(CH3)=NC12H25]}]2 In N,N-dimethyl-formamide at 140℃; for 12h; Heck coupling;99%
With C37H38BrClFeN3Pd; potassium acetate In N,N-dimethyl acetamide at 150℃; for 12h; Heck reaction; Inert atmosphere; regioselective reaction;99%
para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

4-acetylphenylboronic acid
149104-90-5

4-acetylphenylboronic acid

4-acetyl-4'-nitrobiphenyl
135-69-3

4-acetyl-4'-nitrobiphenyl

Conditions
ConditionsYield
With sodium carbonate; palladium on activated charcoal In ethanol at 20℃; for 19h; Suzuki-Miyaura cross-coupling;100%
With palladium 10% on activated carbon; caesium carbonate at 100℃; for 24h; Suzuki-Miyaura coupling; Neat (no solvent);100%
With sodium phosphate dodecahydrate In water; isopropyl alcohol at 20℃; for 23h; Reagent/catalyst; Suzuki-Miyaura Coupling; Inert atmosphere;98%
4-nitrobenzenediazonium tetrafluoroborate
456-27-9

4-nitrobenzenediazonium tetrafluoroborate

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With dibenzo-18-crown-6; potassium bromide; copper(ll) bromide; 1,10-Phenanthroline; copper(I) bromide In acetonitrile at 20℃; for 0.333333h; Sandmeyer bromination;99%
With N-Bromosuccinimide; tetrabutylammonium perchlorate In methanol; N,N-dimethyl-formamide at 20℃; for 1h; Sandmeyer Reaction; Electrochemical reaction;84%
With 1,3-bis-n-butylimidazolium bromide at 80℃; for 0.5h;71%
4-Bromophenylboronic acid
5467-74-3

4-Bromophenylboronic acid

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With nitric acid In 1,2-dichloro-ethane at 70℃; for 16h; Inert atmosphere;98%
With copper(II) nitrate trihydrate; trifluoroacetic acid In ethyl acetate at 100℃; for 3h;96%
With 1,1,1,3',3',3'-hexafluoro-propanol; 2-nitrobenzo[d]isothiazol-3(2H)-one 1,1-dioxide at 60℃; for 19h; Reagent/catalyst; Inert atmosphere; Schlenk technique;96%
2-bromo-5-nitrobenzoic acid
943-14-6

2-bromo-5-nitrobenzoic acid

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With silver carbonate In dimethyl sulfoxide at 120℃; for 16h;97%
With silver carbonate In dimethyl sulfoxide at 120℃;
4-nitrophenylhydrazine hydrochloride
636-99-7

4-nitrophenylhydrazine hydrochloride

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With boron tribromide; dimethyl sulfoxide at 80℃; for 1h;97%
bis(4-bromophenyl)iodonium triflate
139139-81-4

bis(4-bromophenyl)iodonium triflate

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With sodium nitrite In ethyl acetate at 70℃; for 16h; Temperature; Solvent; Sealed tube; regioselective reaction;96%
4-bromo-aniline
106-40-1

4-bromo-aniline

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With 3-chloro-benzenecarboperoxoic acid In toluene for 3h; Reflux;95%
With tert.-butylhydroperoxide In acetonitrile at 60℃; for 4h; Reagent/catalyst; Temperature; Solvent; Schlenk technique;91%
With tert.-butylhydroperoxide; 3 A molecular sieve; zirconium(IV) tert-butoxide In dichloromethane for 1.5h; Ambient temperature;89%
bromobenzene
108-86-1

bromobenzene

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With sodium nitrate In neat (no solvent) at 20℃; for 0.0666667h; Green chemistry;92%
With bismuth(III) nitrate; sulfuric acid; silica gel at 25℃; for 0.0666667h;90%
With tetrammine copper(II) sulphate; nitric acid In dichloromethane; water at 20℃; for 2h; regioselective reaction;85%
4-nitro-aniline
100-01-6

4-nitro-aniline

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With tert.-butylnitrite; tetrabutylammomium bromide; copper(I) bromide; 10-camphorsulfonic acid In acetonitrile at 20℃; for 24h; Reagent/catalyst; Time; Solvent;91%
With tert.-butylnitrite; tetrabutylammomium bromide; toluene-4-sulfonic acid; copper(ll) bromide87%
With tert.-butylnitrite; tetrabutylammomium bromide; toluene-4-sulfonic acid; copper(ll) bromide In acetonitrile at 20℃; for 1h;86%
para-nitrophenyl triflate
17763-80-3

para-nitrophenyl triflate

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With [Cp*Ru(CH3CN)3]OTf; lithium bromide at 100℃; for 12h; Inert atmosphere;91%
With tetrabutylammomium bromide In toluene for 48h; Heating;60%
4-nitrophenylboronic acid
24067-17-2

4-nitrophenylboronic acid

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With sodium nitrite In acetonitrile at 80℃; for 16h; Sealed tube;89%
di-(p-bromophenyl)iodonium trifluoromethanesulfonate

di-(p-bromophenyl)iodonium trifluoromethanesulfonate

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With sodium nitrite In 1,2-dichloro-ethane at 20 - 80℃; Schlenk technique;88%
4-Bromobenzoic acid
586-76-5

4-Bromobenzoic acid

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With nitronium tetrafluoborate; silver carbonate In N,N-dimethyl acetamide at 90℃; for 12h; Inert atmosphere; Schlenk technique; regioselective reaction;84%
With 1,3-disulfonic acid imidazolium nitrate In neat (no solvent) at 50℃; for 0.333333h; Inert atmosphere;77%
4-nitrobenzenediazonium o-benzenedisulfonimide

4-nitrobenzenediazonium o-benzenedisulfonimide

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With tetrabutylammomium bromide; copper In acetonitrile at 20℃; for 0.75h; Substitution;83%
With tetrabutylammomium bromide In acetonitrile at 20℃; for 0.75h; Substitution;77%
Multi-step reaction with 2 steps
1: 86 percent / aq. NaOH / 0.5 h / 0 - 5 °C
2: 83 percent / aq. HBr / acetonitrile / 0.25 h / 60 °C
View Scheme
3,3-dimethyl-1-(4-nitrophenyl)triazene
7227-92-1

3,3-dimethyl-1-(4-nitrophenyl)triazene

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With hydrogen bromide In acetonitrile at 60℃; for 0.25h;83%
1-bromo-2-naphthol
573-97-7

1-bromo-2-naphthol

4-nitrobenzenediazonium o-benzenedisulfonimide

4-nitrobenzenediazonium o-benzenedisulfonimide

A

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

B

para red
6410-10-2

para red

Conditions
ConditionsYield
With sodium hydroxide; tetraethylammonium bromide In acetonitrile at 20℃; for 10h; Product distribution; Further Variations:; Reagents; Reaction partners;A 80%
B 15%
4-nitrobenzenediazonium 4-methylbenzenesulfonate
1947-33-7

4-nitrobenzenediazonium 4-methylbenzenesulfonate

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With potassium bromide In water at 20℃; for 1h;80%
tert-butyl 2-(4-nitrophenyl)diazenecarboxylate
92722-14-0

tert-butyl 2-(4-nitrophenyl)diazenecarboxylate

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With Bromotrichloromethane; trifluoroacetic acid In benzene at 20℃;79%
With Bromotrichloromethane; trifluoroacetic acid In acetonitrile at 80℃; for 0.5h;57%
bromobenzene
108-86-1

bromobenzene

A

2-nitrophenyl bromide
577-19-5

2-nitrophenyl bromide

B

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With nitric acid at 50℃; for 3h;A 20.9%
B 78.2%
With Iron(III) nitrate nonahydrate; phosphorus pentoxide In neat (no solvent) at 20℃; for 6h; Milling; Green chemistry; Overall yield = 93 percent;A 25%
B 68%
With thionyl chloride; bismuth subnitrate In dichloromethane at 20℃; for 9h;A 18%
B 60%
4-bromo-N,N-dimethylaniline
586-77-6

4-bromo-N,N-dimethylaniline

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
ConditionsYield
With tert.-butylhydroperoxide; ammonium iodide; water In dimethyl sulfoxide at 90℃; for 4h; Sealed tube;73%
para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

4-bromo-aniline
106-40-1

4-bromo-aniline

Conditions
ConditionsYield
With copper(I) chloride; potassium borohydride In methanol for 0.166667h; Ambient temperature;100%
With sodium tetrahydroborate In methanol at 60℃; for 3h; Sealed tube;100%
With water; oxalic acid; titanium(IV) oxide for 3h; Wavelength; Irradiation; Inert atmosphere; Sealed tube; Green chemistry; chemoselective reaction;100%
pyrrolidine
123-75-1

pyrrolidine

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

1-(4-nitro-phenyl)-pyrrolidine
10220-22-1

1-(4-nitro-phenyl)-pyrrolidine

Conditions
ConditionsYield
In tetrahydrofuran at 50℃; under 6375510 Torr; for 20h;100%
In tetrahydrofuran at 50℃; under 9000720 Torr; for 20h;100%
With C30H25BrN3PPdS; potassium carbonate In iso-butanol at 100℃; for 24h; Buchwald-Hartwig Coupling; Inert atmosphere;99.4%
1,4-diaza-bicyclo[2.2.2]octane
280-57-9

1,4-diaza-bicyclo[2.2.2]octane

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

1-(4-Nitro-phenyl)-4-aza-1-azonia-bicyclo[2.2.2]octane; bromide
112473-27-5

1-(4-Nitro-phenyl)-4-aza-1-azonia-bicyclo[2.2.2]octane; bromide

Conditions
ConditionsYield
In tetrahydrofuran at 50℃; under 4500360 Torr; for 75h;100%
In tetrahydrofuran at 50℃; under 4500360 Torr; for 20h; Yield given;
phenylacetylene
536-74-3

phenylacetylene

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

4-(phenylethynyl)nitrobenzene
1942-30-9

4-(phenylethynyl)nitrobenzene

Conditions
ConditionsYield
With potassium carbonate In ethanol; water at 65℃; for 8h; Sonogashira Cross-Coupling; Inert atmosphere;100%
With 1,4-diaza-bicyclo[2.2.2]octane; PdCl2[4,4'-bis(n-C10F21CH2OCH2)-2,2'-bipyridine] In N,N-dimethyl-formamide at 140℃; for 0.5h; Catalytic behavior; Sonogashira Cross-Coupling; Microwave irradiation;100%
With copper(l) iodide; triethylamine; triphenylphosphine In water at 60℃; for 24h; Catalytic behavior; Solvent; Reagent/catalyst; Temperature; Time; Sonogashira Cross-Coupling; Schlenk technique; Inert atmosphere;100%
para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

phenol
108-95-2

phenol

4-nitrophenyl phenyl ether
620-88-2

4-nitrophenyl phenyl ether

Conditions
ConditionsYield
With caesium carbonate; copper(I) bromide; 1,1'-azobis(1-cyanocyclohexanenitrile) In N,N-dimethyl-formamide at 100℃; for 1.5h; Reagent/catalyst; Temperature; Solvent; Microwave irradiation; Green chemistry;100%
With potassium fluoride; copper(II) ion; silica gel In dimethyl sulfoxide at 130℃; for 16h; Ullmann diaryl etherification;98%
With caesium carbonate; potassium iodide In N,N-dimethyl-formamide at 120℃; for 22h; Ullmann condensation; Inert atmosphere;95%
para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

phenylboronic acid
98-80-6

phenylboronic acid

1-phenyl-4-nitrobenzene
92-93-3

1-phenyl-4-nitrobenzene

Conditions
ConditionsYield
With sodium carbonate; palladium on activated charcoal In ethanol at 20℃; for 2h; Suzuki-Miyaura cross-coupling;100%
With PdCl*(2-({[(2-methylselanyl)ethyl]imino}methyl)benzenol); potassium carbonate In N,N-dimethyl-formamide at 100℃; for 24h; Suzuki-Miyaura cross-coupling;100%
With 1,4-diaza-bicyclo[2.2.2]octane; caesium carbonate; palladium diacetate In N,N-dimethyl-formamide at 40℃; for 16h; Suzuki-Miyaura cross-coupling;100%
para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

β-naphthol
135-19-3

β-naphthol

4-nitrophenyl 2-naphthyl ether
71311-82-5

4-nitrophenyl 2-naphthyl ether

Conditions
ConditionsYield
With caesium carbonate; copper(I) bromide; 1,1'-azobis(1-cyanocyclohexanenitrile) In N,N-dimethyl-formamide at 100℃; for 0.5h; Microwave irradiation; Green chemistry;100%
With copper(l) iodide; 2-carbomethoxy-3-hydroxyquinoxaline-di-N-oxide; caesium carbonate In N,N-dimethyl-formamide at 100℃; for 12h; Schlenk technique; Inert atmosphere;93%
With potassium carbonate In dimethyl sulfoxide at 80℃; for 12h; Catalytic behavior; Ullmann Condensation; Sealed tube; Schlenk technique;91%
2-methyl-but-3-yn-2-ol
115-19-5

2-methyl-but-3-yn-2-ol

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

2-methyl-4-(4-nitrophenyl)but-3-yn-2-ol
33432-53-0

2-methyl-4-(4-nitrophenyl)but-3-yn-2-ol

Conditions
ConditionsYield
With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine In tetrahydrofuran for 12h; Sonogashira Cross-Coupling; Inert atmosphere; Reflux;100%
With copper(l) iodide; triethylamine; triphenylphosphine at 90℃; for 3h; Sonogashira coupling; Inert atmosphere;97%
With copper(l) iodide; triethylamine; bis-triphenylphosphine-palladium(II) chloride In tetrahydrofuran for 12h; Heating;96%
styrene
292638-84-7

styrene

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

trans-4-nitrostilbene
1694-20-8

trans-4-nitrostilbene

Conditions
ConditionsYield
With tetramethylquanidine; sodium acetate; palladium dichloride In N,N-dimethyl acetamide at 140℃; for 20h; Heck reaction;100%
With 2-n-butyl-1,1,1,3,3-tetramethylguanidine acetate; palladium dichloride at 140℃; for 0.25h;99%
With 0.42C23H20N4O4*2Cl(1-)*Zn(2+)*10.16H2O*0.58Pd(2+)*0.58C23H20N4O4(1-); potassium carbonate In N,N-dimethyl acetamide at 100℃; for 1h; Heck Reaction;99%
acrylic acid n-butyl ester
141-32-2

acrylic acid n-butyl ester

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

(E)-n-butyl 4-nitrocinnamate
86622-84-6, 131061-15-9

(E)-n-butyl 4-nitrocinnamate

Conditions
ConditionsYield
With tetramethylquanidine; sodium acetate; palladium dichloride In N,N-dimethyl acetamide at 140℃; for 20h; Heck reaction;100%
With 2-n-butyl-1,1,1,3,3-tetramethylguanidine acetate; palladium dichloride at 140℃; for 0.25h;100%
With tri-n-propylamine In 1-methyl-pyrrolidin-2-one at 125℃; for 1h; Mizoroki-Heck reaction; Inert atmosphere;100%
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