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
Cas:95-52-3
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryWelcome 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
Cas:95-52-3
Min.Order:1 Metric Ton
Negotiable
Type:Manufacturers
inquiryTechnology: Technology innovation is our eternal pursuit,or we will be left behind.Our technology experts,all from famous universities and institutes,has rich experience and high achievements in chemical research.This makes sure that our technology
high quality Appearance:white powder 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
The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
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
Hebei Yanxi Chemical Co., Ltd. is a professional research, development and production of lead acetate benzene acetamide enterprise backbone members by local well-known entrepreneurs and professional senior engineers in the party's "low car
Cas:95-52-3
Min.Order:1 Metric Ton
FOB Price: $1.0 / 2.0
Type:Trading Company
inquiryOur company was built in 2009 with an ISO certificate.In the past 6 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.O
Cas:95-52-3
Min.Order:1 Kilogram
FOB Price: $1000.0
Type:Lab/Research institutions
inquiryProduct Name 2-Fluorotoluene Synonyms 2-Fluorotoluene;1-Fluor-2-methylbenzol CAS 95-52-3 CAS: 95-52-3 MF: - MW: - EINECS:
Cas:95-52-3
Min.Order:5 Metric Ton
FOB Price: $1.0 / 2.0
Type:Other
inquiryAdvantage : LIDE PHARMACEUTICALS LTD. is a mid-small manufacturing-type enterprise, engaged in pharmaceutical intermediates of R&D, custom-made and production, and also involving trading chemicals for export. We have established the
Cas:95-52-3
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
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
Cas:95-52-3
Min.Order:0 Metric Ton
Negotiable
Type:Lab/Research institutions
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
o-FluorotoluenAppearance:Colorless transparent liquid Storage:Keep away of light, cool place Package:according to customers' requirements Application:pharmaceutical intermediates Transportation:By air(EMS or EUB or FedEx or TNT ect...) or by sea(FOB
Superior quality, moderate price & quick delivery. Appearance:Colorless clear liquid Storage:Store in dry、dark、ventilated place.For medicine , pesticide intermediates Package:25kg/drum, or as per your request. Application:For medicine , pes
95-52-3 Appearance:95%+ Package:R&D,Pilot run Application:95-52-3 Transportation:per client require Port:Express ,Air, Sea
SAGECHEM is a chemical R&D, manufacturing and distribution company in China since 2009, including pharmaceutical intermediates, agrochemical, dyestuff intermediates, organosilicone, API and etc. We also offer a full range of services in custom synthe
Shanghai Massive Chemical Technology Co., Ltd. is engaged in development, production and marketing Specialty Chemicals to satisfy the changing needs of the chemical industry. We specialize in manufacturing high quality of Advanced Intermediates, Sp
Capability on chemical synthesis1. Beijing High-Tech Enterprises2. Strong R&D Team3. 8 years of experiences in R & D of high-tech Catalyst;4. 5000 production techniques, 69 items of national patents, and 360 kinds of products on sales;5. The producti
o-FluorotolueneAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air
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
R & D enterprises have their own stock in stockAppearance:To be subject to the object Package:Customized Application:pharmaceutical intermediates Transportation:Air Port:Shanghai;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
good quality and cheap price Package:25kg/200kg Application:as intermediates Transportation:by courier/sea/air
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
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
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:95-52-3
Min.Order:1 Kilogram
FOB Price: $112.0
Type:Trading Company
inquiryAnsciep 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
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
Supply top quality products with a reasonable price Application:api
Conditions | Yield |
---|---|
With pyridine hydrogenfluoride; sodium nitrite 1.) O deg C, 20 min, 2.) 55 deg C, 1 h; | 99% |
With hydrogen fluoride; sodium nitrite at -1 - 3℃; for 1h; | 99.5% |
Stage #1: o-toluidine With hydrogen fluoride at -15 - 0.5℃; Flow reactor; Large scale; Stage #2: With nitrosylsulfuric acid at -5 - 0.5℃; Flow reactor; Large scale; | 98.1% |
Conditions | Yield |
---|---|
With copper(I) trifluoromethanesulfonate bis(trimethylacetonitrile) complex; silver fluoride In N,N-dimethyl-formamide at 140℃; for 22h; Inert atmosphere; | 96% |
o-fluorobenzyl bromide
A
2-Fluorotoluene
B
9,10-dihydrophenanthrene
C
1,2-bis(2-fluorophenyl)ethane
Conditions | Yield |
---|---|
With magnesium at 600℃; | A 11% B 3% C 80% |
trifluorormethanesulfonic acid
2-methylphenyl diazonium tetrafluoroborate
A
2-Fluorotoluene
B
2-methylphenyl triflate
Conditions | Yield |
---|---|
at 90℃; for 1h; | A n/a B 75% |
2-fluorobenzyl chloride
A
2-Fluorotoluene
B
9,10-dihydrophenanthrene
C
1,2-bis(2-fluorophenyl)ethane
Conditions | Yield |
---|---|
With magnesium at 600℃; | A 7% B 5% C 73% |
toluene-2-diazonium ; hexafluoro phosphate
2-Fluorotoluene
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate at 120 - 125℃; for 1h; | 72% |
Conditions | Yield |
---|---|
With 1,3-bis(2,6-diisopropylphenyl)-2,2-difluoro-2,3-dihydro-1h-imidazole; cesium fluoride; diphenylzinc In 1,4-dioxane at 110℃; for 20h; Product distribution / selectivity; Sealed vial; | 72% |
With 1,3-bis(2,6-diisopropylphenyl)-2,2-difluoro-2,3-dihydro-1h-imidazole; diphenylzinc; cesium fluoride In 1,4-dioxane at 23 - 110℃; for 20.5h; Inert atmosphere; | 87 %Spectr. |
para-chlorotoluene
A
p-fluorotoluene
B
2-Fluorotoluene
C
m-Fluorotoluene
Conditions | Yield |
---|---|
With Al2CuF8 Gas phase; Inert atmosphere; | A 71% B 5% C 10% |
With silver fluoride at 350℃; Product distribution / selectivity; Gas phase; | A 20.8% B 0.6% C 35.8% |
Conditions | Yield |
---|---|
With lithium hydroxide monohydrate; silver trifluoromethanesulfonate; Selectfluor In ethyl acetate at 55℃; Sealed tube; | A 71% B n/a |
Conditions | Yield |
---|---|
With Al2CuF8 Gas phase; Inert atmosphere; | A 60% B 7% |
(2-tolyl)tributyltin
2-Fluorotoluene
Conditions | Yield |
---|---|
With copper(II) bis(trifluoromethanesulfonate); tetrabutylammonium triphenyldifluorosilicate In acetonitrile at 60℃; for 3h; Sealed tube; regiospecific reaction; | 50% |
With copper(I) trifluoromethanesulfonate bis(trimethylacetonitrile) complex; 1-fluoro-2,4,6-trimethylpyridinium trifluoromethanesulfonate In ethyl acetate at 25℃; for 12h; Inert atmosphere; Glovebox; | 76 %Spectr. |
lead(IV) tetraacetate
trifluoroborane diethyl ether
toluene
A
p-fluorotoluene
B
2-Fluorotoluene
C
m-Fluorotoluene
Conditions | Yield |
---|---|
mercury(II) diacetate Stirring of toluene in BF3*Et2O contg. Pb(OAc)4 and overnight at room temp.; GC anal. 13% recovery of toluene.; | A 43% B 12% C 4% |
2-methylphenyl triflate
2-Fluorotoluene
Conditions | Yield |
---|---|
With bis[(trimethylsilyl)methyl](1,5-cyclooctadiene)palladium(II); t-BuBrettPhos; cesium fluoride In toluene at 130℃; for 12h; | 42% |
With bis[(trimethylsilyl)methyl](1,5-cyclooctadiene)palladium(II); t-BuBrettPhos; cesium fluoride In toluene at 130℃; for 12h; | 42 %Chromat. |
Conditions | Yield |
---|---|
With hydrazine hydrate In 1,2-dimethoxyethane for 15h; Heating; | A 29% B 45 % Chromat. |
1-chloro-3-methylbenzene
A
p-fluorotoluene
B
2-Fluorotoluene
C
m-Fluorotoluene
Conditions | Yield |
---|---|
With silver fluoride at 350℃; Product distribution / selectivity; Gas phase; | A 15% B 6.7% C 25.7% |
2-methylchlorobenzene
A
p-fluorotoluene
B
2-Fluorotoluene
C
m-Fluorotoluene
Conditions | Yield |
---|---|
With silver fluoride at 350℃; Product distribution / selectivity; Gas phase; | A 0.5% B 13.9% C 14.4% |
fluorobenzene
Methyl fluoride
A
p-fluorotoluene
B
2-Fluorotoluene
C
m-Fluorotoluene
Conditions | Yield |
---|---|
at 37.5℃; Product distribution; Irradiation; various fluorobenzenes, other conditions; |
Chlorodifluoromethane
A
fluorobenzene
B
p-fluorotoluene
C
2-Fluorotoluene
D
m-Fluorotoluene
E
benzene
Conditions | Yield |
---|---|
With methylcyclopentadiene at 650.9℃; Product distribution; Mechanism; conditions of pulse gas compression, other temperatures; |
Methyl formate
C7H7F*H(1+)
A
2-Fluorotoluene
B
C2H4O2*H(1+)
Conditions | Yield |
---|---|
Thermodynamic data; |
Conditions | Yield |
---|---|
With fluorine In trichlorofluoromethane at -78℃; |
Conditions | Yield |
---|---|
Thermodynamic data; |
toluene
A
2-Fluorotoluene
B
Toluene; compound with GENERIC INORGANIC NEUTRAL COMPONENT
Conditions | Yield |
---|---|
Thermodynamic data; |
Conditions | Yield |
---|---|
With Selectfluor In acetonitrile for 16h; Heating; also fluorination of other aromatic compounds; | A 20 % Spectr. B 60 % Spectr. |
With potassium hydroxide; nitrogen; fluorine In methanol at -40℃; Product distribution; different educt and reagent concentration, different temperatures, different fluorine/nitrogen ratio, different solvents, without or with different additives; | A 57.0 % Chromat. B 32.7 % Chromat. |
With acetyl hypofluorite for 2h; | |
With trifluorormethanesulfonic acid; Selectfluor In dichloromethane at 40℃; for 24h; Fluorination; Title compound not separated from byproducts; |
Conditions | Yield |
---|---|
With fluorine In trichlorofluoromethane at -78℃; for 1h; Rate constant; Product distribution; competitive reaction with benzene, other solvent; | A 29 % Chromat. B 60 % Chromat. C 11 % Chromat. |
With lead(IV) acetate; boron trifluoride diethyl etherate; mercury(II) diacetate Ambient temperature; | A 43 % Chromat. B 12 % Chromat. C 4 % Chromat. |
With caesium fluoroxysulphate; trifluorormethanesulfonic acid In acetonitrile Ambient temperature; Yield given; |
toluene
A
p-fluorotoluene
B
2-Fluorotoluene
C
m-Fluorotoluene
D
benzyl fluoride
Conditions | Yield |
---|---|
With acetyl hypofluorite In acetic acid for 0.0833333h; Ambient temperature; Yield given. Yields of byproduct given; | |
With fluorine In acetonitrile at 0℃; Flow reactor; |
toluene
A
p-fluorotoluene
B
2-Fluorotoluene
C
m-Fluorotoluene
D
2,4-difluorotoluene
Conditions | Yield |
---|---|
With tetrafluoroammonium tetrafluoroborate In hydrogen fluoride at 0℃; Further byproducts given. Title compound not separated from byproducts; | A 15 % Spectr. B 15 % Spectr. C 8 % Spectr. D 30 % Spectr. |
toluene
A
p-fluorotoluene
B
2-Fluorotoluene
C
m-Fluorotoluene
D
2,4-difluorotoluene
Conditions | Yield |
---|---|
With tetrafluoroammonium tetrafluoroborate In hydrogen fluoride at 0℃; Product distribution; | A 15 % Spectr. B 15 % Spectr. C 8 % Spectr. D 30 % Spectr. E 7 % Spectr. |
Conditions | Yield |
---|---|
With tetrafluoroammonium tetrafluoroborate In hydrogen fluoride at 0℃; Further byproducts given. Title compound not separated from byproducts; | A 15 % Spectr. B 15 % Spectr. C 8 % Spectr. D 7 % Spectr. |
Conditions | Yield |
---|---|
With caesium fluoroxysulphate In acetonitrile at 25℃; Product distribution; Rate constant; reagents ratio, presence of 1,3,5-trinitrobenzene; | A 2 % Chromat. B 4 % Chromat. C 67 % Chromat. |
With caesium fluoroxysulphate In acetonitrile Ambient temperature; Yield given. Yields of byproduct given; |
Conditions | Yield |
---|---|
Stage #1: 2-Fluorotoluene With sec.-butyllithium In tetrahydrofuran at -78℃; for 0.5h; Stage #2: carbon dioxide In tetrahydrofuran under 760.051 Torr; | 100% |
Stage #1: 2-Fluorotoluene With n-butyllithium Metallation; Stage #2: carbon dioxide Carboxylation; |
Conditions | Yield |
---|---|
With caesium carbonate In N,N-dimethyl acetamide at 210℃; for 12h; Microwave irradiation; | 100% |
Conditions | Yield |
---|---|
With triethanolamine; 2,2'-azobis(isobutyronitrile); chlorine at 90 - 115℃; for 5h; | 99% |
Conditions | Yield |
---|---|
With di-tert-butyl peroxide; C11H23N2(1+)*Br4Fe(1-) at 110℃; for 24h; | 98% |
Conditions | Yield |
---|---|
With 1-[2-(diphenylphosphino)phenyl]ethanol; bis(acetylacetonate)nickel(II) In diethyl ether at 20℃; for 5h; | 96% |
With 1,3-bis(2,6-diisopropylphenyl)-4,5-dihydro-1H-imidazolium tetrafluoroborate; Ni(acac) In tetrahydrofuran at 20℃; for 18h; Kumada-Corriu cross-coupling; | 53 % Chromat. |
Conditions | Yield |
---|---|
Stage #1: 2-Fluorotoluene; phenylmagnesium bromide; 1-[2-(diphenylphosphino)phenyl]ethanol; bis(acetylacetonate)nickel(II) In diethyl ether for 5h; Stage #2: With methanol In diethyl ether Product distribution / selectivity; | 96% |
Stage #1: 2-Fluorotoluene; phenylmagnesium bromide; bis(acetylacetonate)nickel(II); ((2-hydroxymethyl)phenyl)diphenylphosphine In diethyl ether for 48h; Stage #2: With methanol In diethyl ether Product distribution / selectivity; | 95% |
With C28H32ClN2NiP In tetrahydrofuran at 20℃; for 24h; Time; Schlenk technique; Inert atmosphere; | 16 %Chromat. |
Conditions | Yield |
---|---|
With C26H24ClN2NiP*0.1C7H8 In toluene at 25℃; for 24h; Kumada Cross-Coupling; Schlenk technique; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
With C23H40Br2N2NiO5P; magnesium In tetrahydrofuran at 60℃; for 12h; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
With Xylaria polymorpha laccase; 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonate) diammonium salt In 1,4-dioxane at 20℃; for 1.91667h; pH=4.5; Green chemistry; Enzymatic reaction; | 94% |
With laccase of Pleurotus ostreatus MTCC-1801; 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt In 1,4-dioxane at 20℃; pH=4.5; Enzymatic reaction; | 90% |
With tert.-butylhydroperoxide; C29H25Cl2N4Ru(1+)*F6P(1-) In acetonitrile at 60℃; for 2h; Schlenk technique; Inert atmosphere; | 74% |
ferrocene
2-Fluorotoluene
η-pentadienyl-η-1,2-fluoromethylbenzeneiron(II) hexafluorophosphate
Conditions | Yield |
---|---|
With aluminium trichloride; aluminium In water other Radiation; 0.02 mol metal addn. to arene, Fe- and Al-salts mixt. in 1,2,4-C6H3Cl3 (ratio arene:Fe:AlCl3:Al=2:1:2:1.1), homogenization (stirring), mixt. irradiation in microwave oven (850 W) for 3 min, ice addn. (AlCl3 decompn.), filtration, filtrate washing (Et2O); filtration, treating with aq. NH4-salt, ppt. filtration off through sinter, washing (i-PrOH, Et2O); elem. anal.; | 94% |
2-Fluorotoluene
p-methoxybenzyl chloride
1-methyl-2-(4-methoxybenzyl) benzene
Conditions | Yield |
---|---|
With Ni(PPh3)(1,3-di-tert-butylimidazol-2-ylidene)Br2; magnesium In tetrahydrofuran at 0 - 35℃; for 24h; Schlenk technique; Inert atmosphere; | 93% |
Conditions | Yield |
---|---|
Stage #1: 3-methylamino-1-phenylpropan-1-ol With potassium hydroxide In Triethylene glycol dimethyl ether; toluene at 20 - 120℃; for 1h; Large scale; Stage #2: 2-Fluorotoluene In Triethylene glycol dimethyl ether; toluene for 3h; Large scale; Stage #3: (S)-Mandelic acid at 20 - 75℃; for 1h; Temperature; Large scale; | 93% |
Conditions | Yield |
---|---|
With di-tert-butyl peroxide; 1,3-di-tert-butylimidazolium at 130℃; for 24h; Green chemistry; | 93% |
Conditions | Yield |
---|---|
With di-tert-butyl peroxide; 1,3-di-tert-butylimidazolium at 130℃; for 24h; | 93% |
2-Fluorotoluene
(+/-)-atomoxetine
Conditions | Yield |
---|---|
Stage #1: 3-methylamino-1-phenylpropan-1-ol With potassium hydroxide In dimethyl sulfoxide at 110℃; Stage #2: 2-Fluorotoluene In dimethyl sulfoxide at 145 - 147℃; for 1h; Heating / reflux; | 92.7% |
2-Fluorotoluene
4-methoxyphenyl magnesium bromide
4'-methoxy-2-methylbiphenyl
Conditions | Yield |
---|---|
Stage #1: 2-Fluorotoluene With Ni(PPh3)(1,3-di-tert-butylimidazol-2-ylidene)Br2 In tetrahydrofuran at 0℃; for 0.0333333h; Inert atmosphere; Schlenk technique; Stage #2: 4-methoxyphenyl magnesium bromide In tetrahydrofuran at 0 - 25℃; for 10h; Inert atmosphere; Schlenk technique; | 92% |
With palladium diacetate; DavePhos In 1,2-dimethoxyethane at 80℃; for 12h; | 73% |
Conditions | Yield |
---|---|
Stage #1: 2-Fluorotoluene With C78H70Al2Cl4N6P4Rh2; magnesium; ethylene dibromide In tetrahydrofuran at 20℃; for 22h; Inert atmosphere; Glovebox; Stage #2: carbon dioxide In tetrahydrofuran at 20℃; under 760.051 Torr; for 0.5h; | 92% |
Conditions | Yield |
---|---|
With aluminum (III) chloride In chloroform at -5 - 20℃; for 2h; Solvent; Reagent/catalyst; Temperature; | 91% |
With aluminium trichloride In dichloromethane at 20℃; for 24h; Friedel-Krafts reaction; | 82% |
With aluminium trichloride | |
Stage #1: 2-Fluorotoluene; acetyl chloride With aluminum (III) chloride In dichloromethane at 20℃; for 26h; Reflux; Stage #2: With water; sodium carbonate In dichloromethane | |
With aluminum (III) chloride In dichloromethane at 20℃; for 26h; Reflux; |
Conditions | Yield |
---|---|
With cesium fluoride; lithium hexamethyldisilazane at 110℃; for 12h; Reagent/catalyst; Temperature; Green chemistry; | 90% |
With cesium fluoride; lithium hexamethyldisilazane at 110℃; for 12h; Reagent/catalyst; Concentration; Sealed tube; Inert atmosphere; | 90% |
2-Fluorotoluene
(R)-N-methyl-3-phenyl-3-hydroxypropylamine
(R)-tomoxetine
Conditions | Yield |
---|---|
Stage #1: (R)-N-methyl-3-phenyl-3-hydroxypropylamine With potassium hydroxide In dimethyl sulfoxide at 130℃; for 1h; Stage #2: 2-Fluorotoluene In dimethyl sulfoxide at 130℃; | 89.51% |
Stage #1: (R)-N-methyl-3-phenyl-3-hydroxypropylamine With sodium hydride In dimethyl sulfoxide for 0.25h; Stage #2: With Potassium benzoate In dimethyl sulfoxide at 50 - 55℃; for 1h; Stage #3: 2-Fluorotoluene In dimethyl sulfoxide at 50 - 120℃; for 6.25 - 7.25h; | |
With potassium tert-butylate In dimethyl sulfoxide at 60℃; for 8h; |
2-Fluorotoluene
4-tert-butyl benzonitrile
2-(4-(tert-butyl)phenyl)-1H-indole
Conditions | Yield |
---|---|
With cesium fluoride; lithium hexamethyldisilazane at 110℃; for 12h; Sealed tube; Inert atmosphere; | 89% |
Conditions | Yield |
---|---|
With 2C2H3F3O*BF3; potassium nitrate at 20℃; for 5h; | 88% |
With nitric acid | |
With nitric acid; Nitrogen dioxide | |
With nitric acid |
Conditions | Yield |
---|---|
With bis(tricyclohexylphosphine)nickel(II) dichloride In tetrahydrofuran at 50℃; for 24h; Inert atmosphere; | 88% |
2-Fluorotoluene
Conditions | Yield |
---|---|
In 1,2-dichloro-ethane at 90℃; for 18h; Inert atmosphere; | 88% |
2-Fluorotoluene
Conditions | Yield |
---|---|
With potassium tert-butylate; 2,2,6,6-tetramethylpiperidinyl-lithium at -40℃; for 18h; Glovebox; Inert atmosphere; | 88% |
Conditions | Yield |
---|---|
With cesium fluoride; lithium hexamethyldisilazane In 1,4-dioxane at 110℃; for 12h; Green chemistry; | 88% |
With cesium fluoride; lithium hexamethyldisilazane In 1,2-dimethoxyethane at 110℃; for 12h; Solvent; Sealed tube; Inert atmosphere; | 88% |
2-Fluorotoluene
bis(pinacol)diborane
2-methylphenylboronic acid pinacol ester
Conditions | Yield |
---|---|
With bis(1,5-cyclooctadiene)nickel (0); copper(l) iodide; cesium fluoride; tricyclohexylphosphine In toluene at 80℃; for 24h; Inert atmosphere; | 87.6% |
With chlorobis(tricyclohexylphosphine)copper(I); cesium fluoride In toluene at 80℃; for 24h; | 79% |
With tetramethylammonium fluoride; 2-mercaptopyridine sodium salt In acetonitrile at 30 - 35℃; for 24h; Irradiation; Inert atmosphere; | 57% |
Conditions | Yield |
---|---|
In 1,4-dioxane at 90℃; for 16h; | 86% |
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