Items Standard Result Appearance Light yellow to green or light brown crystallization light brown crystallization
Cas:100-02-7
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inquiry1,ISO Certificate 2,Factory price 3,Free sample and Fast delivery Appearance:Yellow to brown crystal Storage:All products should be stored at a dry and ventilated location away from fire and other dangerous goods, and should avoid direct sunlight.
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As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem’s R&D center offer custom synthesis according to the contract research and development services for the fine c
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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
4-Nitrophenol Basic information Product Name: 4-Nitrophenol Synonyms: 1-Hydroxy-4-nitrobenzene;4-hydroxy-1-nitrobenzene;4-Nitrofenol;4-nitro-pheno;Mononitrophenol;NCI-C55992;Niphen;Paran
Product Name 4-Nitrophenol Synonyms 1-Hydroxy-4-nitrobenzene;4-hydroxy-1-nitrobenzene;4-Nitrofenol;4-nitro-pheno;Mononitrophenol;NCI-C55992;Niphen;Paranitrofenol CAS 100-02-7
Our company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At present
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inquiryHangzhou Keying Chem Co., Ltd. Is a comprehensive enterprise, dedicated to the development, production and marketing of chemicals. As a technology innovative and service professional enterprise, Our company mainly engages in global pharmaceutical,
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inquiryJ&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
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
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inquirySuperior quality, moderate price & quick delivery. Appearance:Yellow to brown crystals Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:25kg/drum or as per your request. Application:Used in the manufacturing of
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inquiryProduct name: Para-Nitrophenol CAS No.:100-02-7 Molecule Formula:C6H5NO3 Molecule Weight:138.10 Purity: 93.0% Package: 25kg/drum Description:Yellow to brown crystalline powder Manufacture Standards:Enterprise Standard
Cas:100-02-7
Min.Order:1 Kilogram
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inquiryLocated 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
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
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
high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Hunan chemfish Pharmaceutical co.,Ltd.located in Lugu High-tech industral park ,Hunan province . with its own R&D center and more than 10000㎡manufacture plant . Chemfish owns 40 reactors from 1000L to 8000L. With complete auxiliary equipment as
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
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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
Name 4-Nitrophenol Synonyms p-Nitrophenol; 1-Hydroxy-4-nitrobenzene Molecular Structure Molecular Formula
4-Nitrophenol,CAS 100-02-7 Application:4-Nitrophenol,CAS 100-02-7
1,we produce and sell good chemicals around the world. 2,our success rate is about 95%. this means, if customer order is accepted, the probability that the customer will obtain the ordered substances, is 95%. 3,our staff consists of highl
4-Nitrophenol,CAS 100-02-7Appearance:Yellow to brown crystal Storage:keep in dry place Package:Aluminum Foil Bag or as your requirement Application:100-02-7 Transportation:By express (Door to door) such as FEDEX, DHL, EMS for small amount. By air(ai
Cas:100-02-7
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryhigh 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
Conditions | Yield |
---|---|
With aminomethyl resin-supported N-propylbarbituric acid; tetrakis(triphenylphosphine) palladium(0) In tetrahydrofuran at 20℃; | 100% |
With chloro-trimethyl-silane; sodium cyanoborohydride In acetonitrile at 20℃; for 0.25h; ether cleavage; | 95% |
With sodium tetrahydroborate; tetrakis(triphenylphosphine) palladium(0) In tetrahydrofuran for 1h; | 94% |
Conditions | Yield |
---|---|
sodium hydrogen sulfate; silica gel In dichloromethane at 20℃; for 1h; | 100% |
With diphosphorus tetraiodide In dichloromethane at 0℃; for 0.75h; | 92% |
With bismuth(III) chloride In water; acetonitrile at 50℃; for 3h; | 92% |
With Montmorillonite K 10 In benzene at 50℃; for 72h; | 20% |
trans-2-(p-nitrophenoxy)-6-carboxytetrahydropyran
4-nitro-phenol
Conditions | Yield |
---|---|
With sodium hydroxide; potassium chloride at 50℃; Rate constant; Mechanism; var. pH; other acetals; other solvent; rate constant vs. pH; | 100% |
Conditions | Yield |
---|---|
silica gel; toluene-4-sulfonic acid In water; toluene at 80℃; for 8h; | 100% |
With ammonium acetate In methanol at 20℃; for 2h; | 99% |
With Vigna unguiculata powder In water; isopropyl alcohol at 30℃; for 72h; | 99% |
4-nitrophenyl methylsulphonylmethanesulphonate
benzylamine
A
4-nitro-phenol
Conditions | Yield |
---|---|
With pH 13 In water at 25℃; | A n/a B 100% |
With potassium hydroxide at 25℃; Rate constant; also with benzylamine buffers; var. conc.; |
4-nitro-phenol
Conditions | Yield |
---|---|
With potassium hydroxide In methanol at 20℃; for 24h; | 100% |
tert-Butyl 4-nitrophenyl carbonate
4-nitro-phenol
Conditions | Yield |
---|---|
With erbium(III) triflate In ethanol for 25h; Microwave irradiation; | 100% |
With methanol; carbon tetrabromide; triphenylphosphine for 12h; Reflux; | 92% |
With zinc diacetate; water-d2; N-ethyl-N,N-diisopropylamine; tris(2-benzylaminoethyl)amine In dimethylsulfoxide-d6 at 21.84℃; Kinetics; Reagent/catalyst; |
4-nitrophenylboronic acid
4-nitro-phenol
Conditions | Yield |
---|---|
With water; oxygen; sodium sulfite at 50℃; for 1h; Green chemistry; | 100% |
With N-ethyl-N,N-diisopropylamine In water; acetonitrile at 20℃; for 30h; Irradiation; Green chemistry; | 99% |
With N-ethyl-N,N-diisopropylamine In water; acetonitrile for 48h; Irradiation; | 99% |
Conditions | Yield |
---|---|
With water; sodium hydroxide at 150℃; for 0.1h; Autoclave; | 100% |
Stage #1: 4-nitro-aniline With tetrafluoroboric acid In water at 20℃; for 0.0333333h; Stage #2: With sodium nitrite In water at 0℃; for 0.5h; Stage #3: With copper(I) oxide; copper(II) sulfate In water at 0 - 20℃; for 0.5h; | 87% |
Stage #1: 4-nitro-aniline With sulfuric acid In water Stage #2: With sulfuric acid; sodium nitrite In water at 0 - 5℃; for 0.166667h; Heating; | 60% |
Conditions | Yield |
---|---|
With arylsulfate sulfotransferase from Desulfitobacterium hafniense In acetone at 30℃; for 96h; pH=9; Kinetics; pH-value; Green chemistry; Enzymatic reaction; regioselective reaction; | A n/a B 100% |
Conditions | Yield |
---|---|
With β-D-glucose; copper(II) acetate monohydrate; potassium hydroxide In water; dimethyl sulfoxide at 20 - 120℃; for 24h; | 99% |
With tetra(n-butyl)ammonium hydroxide; water at 100℃; for 4h; | 96% |
Stage #1: 4-chlorobenzonitrile With sodium hydroxide In water at 170℃; under 3750.38 Torr; for 8h; Inert atmosphere; Stage #2: With hydrogenchloride In water at 80℃; for 1h; pH=1.5; Temperature; pH-value; Pressure; Reagent/catalyst; | 96.7% |
Conditions | Yield |
---|---|
Stage #1: para-nitrophenyl bromide With potassium hydroxide; tris-(dibenzylideneacetone)dipalladium(0); 2-((di-adamantan-1-yl)phosphaneyl)-1-(2,6-diisopropylphenyl)-1H-imidazole In 1,4-dioxane; water at 100℃; for 20h; Inert atmosphere; Stage #2: With hydrogenchloride In 1,4-dioxane; water at 20℃; Inert atmosphere; | 99% |
With β-D-glucose; copper(II) acetate monohydrate; potassium hydroxide In water; dimethyl sulfoxide at 20 - 120℃; for 24h; | 99% |
With dicyclohexyl-(2′,4′,6′-triisopropyl-3,6-dimethoxy-[1,1′-biphenyl]-2-yl)phosphine; boric acid; palladium diacetate; caesium carbonate In 1-methyl-pyrrolidin-2-one at 80℃; for 24h; Schlenk technique; Inert atmosphere; | 99% |
1-[(2-methoxyethoxy)methoxy]-4-nitrobenzene
4-nitro-phenol
Conditions | Yield |
---|---|
sodium hydrogen sulfate; silica gel In dichloromethane at 20℃; for 1.5h; | 99% |
With diphosphorus tetraiodide In dichloromethane 0 degC, 25 min and room temp., 5 min; | 92% |
Conditions | Yield |
---|---|
With 2-(methylsulfonyl)ethyl alcohol; sodium hydride In N,N-dimethyl-formamide at 0 - 20℃; | 99% |
With sodium hydroxide In dimethyl sulfoxide at 80℃; for 12h; | 90% |
With methyl propargyl alcohol; potassium tert-butylate In dimethyl sulfoxide at 125℃; for 0.0333333h; microwave irradiation; | 78% |
Conditions | Yield |
---|---|
In water; N,N-dimethyl-formamide at 20℃; for 0.5h; | 99% |
para-nitrophenyl triflate
4-nitro-phenol
Conditions | Yield |
---|---|
With tetraethylammonium hydroxide In 1,4-dioxane at 20℃; for 1h; | 99% |
Conditions | Yield |
---|---|
With β-D-glucose; copper(II) acetate monohydrate; potassium hydroxide In water; dimethyl sulfoxide at 20 - 120℃; for 16h; | 99% |
With copper(I) oxide; N-phenylpicolinamide; sodium hydroxide In water; dimethyl sulfoxide at 160℃; for 0.166667h; Microwave irradiation; | 98% |
With basolite C300; potassium hydroxide In water; dimethyl sulfoxide at 125℃; for 12h; | 96% |
2-(4-nitrophenoxy)tetrahydropyran
4-nitro-phenol
Conditions | Yield |
---|---|
With montmorillonite K-10 In methanol at 40 - 50℃; for 0.4h; | 98% |
With methanol; zirconium(IV) chloride at 20℃; for 5h; | 86% |
With acid-washed bentonite In acetone at 40 - 50℃; for 0.333333h; | 86.7% |
Conditions | Yield |
---|---|
With lithium chloride In N,N-dimethyl-formamide for 24h; Heating; | 98% |
With water; hydrogen bromide; Aliquat 336 at 105℃; for 3.5h; Catalytic behavior; | 97% |
With copper(I) oxide; sodium methylate In methanol at 185℃; for 12h; Autoclave; | 87% |
tert-butyldimethyl(4-nitrophenoxy)silane
4-nitro-phenol
Conditions | Yield |
---|---|
With water; potassium carbonate In ethanol at 75℃; for 2h; | 98% |
With triethylamine N-oxide In methanol for 0.5h; | 96% |
With hafnium tetrakis(trifluoromethanesulfonate) In methanol at 20℃; for 10h; | 96% |
Conditions | Yield |
---|---|
With cerium(III) chloride; sodium iodide In acetonitrile for 4h; tosylate cleavage; Heating; | 98% |
With tetraethylammonium hydroxide In 1,4-dioxane at 20℃; for 24h; | 92% |
With potassium fluoride on basic alumina for 0.1h; Substitution; microwave irradiation; | 86% |
C22H15NO5
4-nitro-phenol
Conditions | Yield |
---|---|
With (triphenylphosphine)gold(I) chloride; silver trifluoromethanesulfonate In ethanol; benzene at 20℃; for 0.5h; | 98% |
p-nitrophenyl sulfate
Leu-enkephalin
A
4-nitro-phenol
B
sulfated [Leu5]-enkephalin
Conditions | Yield |
---|---|
With arylsulfate sulfotransferase from Desulfitobacterium hafniense In aq. buffer at 30℃; for 144h; pH=8; Green chemistry; Enzymatic reaction; regioselective reaction; | A n/a B 98% |
Conditions | Yield |
---|---|
With methylene blue; N-ethyl-N,N-diisopropylamine In water; acetonitrile at 20℃; for 7h; Schlenk technique; Irradiation; | 98% |
4-(4'-Nitrophenoxy)-2,3,5,6-tetrafluoropyridine
4-nitro-phenol
Conditions | Yield |
---|---|
With potassium fluoride; 18-crown-6 ether; Methyl thioglycolate In water; acetonitrile at 50℃; for 2h; | 98% |
4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nitrobenzene
4-nitro-phenol
Conditions | Yield |
---|---|
With [Rh2(bpy)2(μ-OAc)2(OAc)2]; oxygen; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide under 760.051 Torr; for 18h; Irradiation; | 98% |
With dihydrogen peroxide In ethanol at 20℃; for 0.5h; pH=9.2; |
p-nitrophenyl methanesulfonate
4-nitro-phenol
Conditions | Yield |
---|---|
With tetraethylammonium hydroxide In 1,4-dioxane at 20℃; for 3h; | 97% |
With sodium azide; copper(ll) sulfate pentahydrate; water; sodium carbonate; sodium L-ascorbate; L-proline In dimethyl sulfoxide at 70℃; for 24h; | 71% |
4<(2-methyl-2-propenyl)oxy>-1-nitrobenzene
4-nitro-phenol
Conditions | Yield |
---|---|
With potassium hydroxide In methanol at 20℃; for 24h; | 97% |
A
4-nitro-phenol
Conditions | Yield |
---|---|
With Dess-Martin periodane In chloroform-d1 for 0.333333h; | A 87% B 97% |
Conditions | Yield |
---|---|
With triethylamine In water; acetonitrile at 25℃; for 7h; Kinetics; Reagent/catalyst; | A n/a B 96% |
With triethylamine hydrochloride; triethylamine In water; acetonitrile at 25℃; Rate constant; different Et3N concentrations and compositions of solvent mixtures; | |
With sodium ethanolate In ethanol at 25℃; Kinetics; Further Variations:; Reagents; Elimination; |
isocyanate de chlorosulfonyle
4-nitro-phenol
N-<<(4-nitrophenyl)oxy>carbonyl>sulfamyl chloride
Conditions | Yield |
---|---|
In diethyl ether for 2h; | 100% |
With benzene | |
In benzene | |
In dichloromethane at 20℃; for 1.5h; | |
With benzene |
Conditions | Yield |
---|---|
With benzyltriphenylphosphonium peroxodisulfate; potassium bromide In acetonitrile for 8.5h; Heating; | 100% |
With N-benzyl-N,N-dimethyl anilinium peroxodisulfate; potassium bromide In acetonitrile for 8h; Reflux; regioselective reaction; | 97% |
With N-Bromosuccinimide; fluorosulphonic acid In acetonitrile at 20℃; for 48h; | 95% |
Conditions | Yield |
---|---|
With copper(I) chloride; potassium borohydride In methanol for 0.166667h; Ambient temperature; | 100% |
With palladium diacetate; carbon monoxide; triphenylphosphine In water; acetic acid at 56℃; under 532 Torr; for 14h; | 100% |
With hydrazine hydrate In ethanol at 80℃; | 100% |
Conditions | Yield |
---|---|
K5 In acetonitrile at 20℃; for 0.333333h; | 100% |
With SBA-15-Ph-Pr-SO3H at 20℃; for 0.833333h; | 100% |
With magnesium(II) perchlorate at 20℃; for 1.5h; | 99% |
Conditions | Yield |
---|---|
With pyridine at 0 - 20℃; Inert atmosphere; | 100% |
With 4-(dimethylamino)pyridine hydrochloride In toluene at 110℃; for 6h; | 98% |
With sodium hydride In tetrahydrofuran at 20℃; for 1h; | 97% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 0.75h; | 100% |
With triethylamine In dichloromethane at 0 - 20℃; | 98% |
With triethylamine In ethyl acetate at 0 - 20℃; for 0.166667h; Green chemistry; | 97% |
4-nitro-phenol
p-toluenesulfonyl chloride
4-nitrophenyl 4-methylbenzenesulfonate
Conditions | Yield |
---|---|
Stage #1: 4-nitro-phenol; p-toluenesulfonyl chloride With potassium carbonate In acetone at 20 - 25℃; for 2.5h; Stage #2: With hydrogenchloride In water; acetone | 100% |
With triethylamine In dichloromethane at 20℃; for 24h; Inert atmosphere; | 99% |
With potassium carbonate for 0.0833333h; microwave irradiation; | 98% |
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran for 1h; Ambient temperature; | 100% |
With triethylamine In tetrahydrofuran at 0℃; for 1h; | 100% |
In 1,4-dioxane; pyridine for 2h; Ambient temperature; | 83% |
With iodine; magnesium; benzene |
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran for 1h; Ambient temperature; | 100% |
With triethylamine In tetrahydrofuran at 0℃; for 1h; | 100% |
In 1,4-dioxane; pyridine for 2h; Ambient temperature; | 65% |
With iodine; magnesium; benzene |
Conditions | Yield |
---|---|
for 20h; Heating; | 100% |
for 16h; Heating; |
Conditions | Yield |
---|---|
With triethylamine In diethyl ether for 0.5h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
With triethylamine In diethyl ether at 0℃; for 0.5h; | 100% |
Conditions | Yield |
---|---|
With triethylamine In diethyl ether at 0℃; for 0.5h; | 100% |
4-nitro-phenol
fluorodinitroacetonitrile
p-nitrophenyl fluorodinitroacetimidate
Conditions | Yield |
---|---|
In diethyl ether; dichloromethane at 60℃; under 7500600 Torr; for 55h; | 100% |
4-nitro-phenol
N-Cbz-L-Phe
N-benzyloxycarbonyl-L-phenylalanine p-nitrophenyl ester
Conditions | Yield |
---|---|
With N,N'-Bis(2-oxo-3-oxazolidinyl)phosphorodiamidic azide; triethylamine In dichloromethane | 100% |
With pyridine; 2,6-di-tert-butyl-4-methyl-phenol In benzene for 12h; | 81% |
With pyridine; diphenyl hydrogen phosphite; mercury dichloride |
4-nitro-phenol
dabsyl chloride
4-(4-Dimethylamino-phenylazo)-benzenesulfonic acid 4-nitro-phenyl ester
Conditions | Yield |
---|---|
With carbonate-bicarbonate buffer In acetone; acetonitrile 1.) 15 min, 2.) reflux; | 100% |
With carbonate-bicarbonate buffer In acetone for 0.5h; Heating; |
4-nitro-phenol
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide In 1,4-dioxane | 100% |
4-nitro-phenol
3-<(benzyloxycarbonyl)aminomethyl>benzoic acid
p-nitrophenyl 3-<(benzyloxycarbonyl)aminomethyl>benzoate
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide | 100% |
4-nitro-phenol
<2,6-2H2>-4-nitrophenol
Conditions | Yield |
---|---|
With water-d2; sulfuric acid-d2 at 120℃; for 48h; | 100% |
With water-d2; hydrogen chloride at 175℃; for 0.333333h; Microwave irradiation; | 82% |
With water-d2; hydrogen chloride for 90h; Heating; | 2.1 g |
With sulfuric acid-d2 at 120℃; sealed tube; |
4-nitro-phenol
p-nitrophenolate
Conditions | Yield |
---|---|
With NaH-cryptand<2.2.1) In tetrahydrofuran for 0.00833333h; other reagents, other times, other solvent, other yields; | 100% |
With NaH-cryptand<2.2.1> In tetrahydrofuran for 0.00833333h; | 100% |
With N-butylamine In dimethyl sulfoxide; benzene at 25℃; Equilibrium constant; ionization in solvent mixtures with different ratio; |
4-nitro-phenol
2-(4-(benzyloxy)-1H-indol-3-yl)acetic acid
4-Nitrophenyl <(4-Benzyloxy)-1H-indol-3-yl>acetate
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide In dichloromethane for 1h; Ambient temperature; | 100% |
With dicyclohexyl-carbodiimide In ethyl acetate 1) ice-bath, 1 h, 2) r.t., 18 h; | 57.7% |
4-nitro-phenol
chloromethyl methyl ether
1-(methoxymethoxy)-4-nitrobenzene
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; Cooling with ice; | 100% |
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0 - 20℃; | 89% |
(i) NaOEt, EtOH, toluene, (ii) /BRN= 505943/; Multistep reaction; |
Conditions | Yield |
---|---|
With t-butyl bromide; triethylamine at 35℃; for 24h; | 100% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone; toluene for 24h; Williamson Ether Synthesis; Reflux; | 100% |
Stage #1: 4-nitro-phenol With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 0.5h; Inert atmosphere; Stage #2: propargyl bromide In N,N-dimethyl-formamide at 20℃; for 10h; Inert atmosphere; | 100% |
Stage #1: 4-nitro-phenol With potassium carbonate In acetonitrile at 20℃; for 0.166667h; Stage #2: propargyl bromide In acetonitrile Reflux; | 100% |
4-nitro-phenol
1,1,3,3-tetramethyldisilazane
Dimethyl-(4-nitro-phenoxy)-silane
Conditions | Yield |
---|---|
100% | |
at 20 - 160℃; for 2h; Inert atmosphere; |
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