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:598-73-2
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inquiryThe 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
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Cas:598-73-2
Min.Order:5 Kiloliter
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Type:Manufacturers
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
Cas:598-73-2
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inquiryZibo 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
Cas:598-73-2
Min.Order:10 Gram
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Type:Lab/Research institutions
inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
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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
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inquiryBROMOTRIFLUOROETHYLENE Package:as requirements Application:Electronicgases
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
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Cas:598-73-2
Min.Order:10 Milligram
Negotiable
Type:Lab/Research institutions
inquiryMore than 8 years chemical exporting experience. We have produced chemical more than 8 years., 90% products are for export . More than 8 years chemical exporting experience. best service and unbeatable price! Appearance:Off white to slight yellow s
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Min.Order:1 Metric Ton
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Type:Trading Company
inquiryUnited Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat
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Type:Lab/Research institutions
inquiryEthene,1-bromo-1,2,2-trifluoro- Storage:keep in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/pharma intermediate Transportation:By Sea,by Air,By courier like DHL or Fedx. Port:Shanghai/Shenzhen
Supply top quality products with a reasonable price Application:api
Debyesci is here who supplied several kinds of chemical products to global pharmaceutical, drug discovery, agrochemical and biotechnology industries for four yearsOur key scientific leadership team has gained experience in top research and developmen
Manufacturer,strong R&D,professional team Storage:Store in a cool, dry place. Store in a tightly closed container. Package:according to your requirement Application:ZhiShang Chemical is owned by ZhiShang Group, is a professional new-type chemicals en
high purity Application:Drug intermediates Materials intermediates and active molecules
Conditions | Yield |
---|---|
With potassium hydroxide | |
With potassium hydroxide | |
With potassium hydroxide; water at 76℃; | |
With pyrographite; potassium nitrate at 20 - 400℃; for 6h; Reagent/catalyst; Temperature; Inert atmosphere; |
Conditions | Yield |
---|---|
Irradiation; radiation > 237 nm; |
3-bromo-3-(trifluoromethyl)diazirine
A
2-bromo-1,1,1-trifluoroethane
B
1-bromo-1,2,2-trifluoroethene
Conditions | Yield |
---|---|
Irradiation; | |
Irradiation; radiation > 330 nm; |
Conditions | Yield |
---|---|
at 120℃; |
1-bromo-1,2,2-trifluoroethene
Conditions | Yield |
---|---|
With ethanol; potassium acetate; potassium carbonate | |
With sodium ethanolate |
(pentafluoro ethyl) magnesiumbromide
A
1,1-dibromo-2,2-difluoroethylene
B
1-bromo-1,2,2-trifluoroethene
C
Iodotrifluoroethylene
Conditions | Yield |
---|---|
In diethyl ether thermal decompn. on warming from -40°C to 20°C; | |
In diethyl ether thermal decompn. on warming from -40°C to 20°C; |
(1,2-dibromotrifluoroethyl)pentafluorosulfur(VI)
A
fluorosulfonyl fluoride
B
1-bromo-1,2,2-trifluoroethene
C
(trifluoroethenyl)pentafluorosulfur(VI)
Conditions | Yield |
---|---|
With Cu with Cu powder, 188°C; |
N(C4H9)4(1+)*CF2CFBF3(1-)=N(C4H9)4[CF2CFBF3]
A
1-bromo-1,2,2-trifluoroethene
B
[Bu4N][CF2BrCFBrBF3]
Conditions | Yield |
---|---|
With bromine In dichloromethane at 20℃; for 66h; |
N(C4H9)4(1+)*CF2CFBF3(1-)=N(C4H9)4[CF2CFBF3]
A
bromopentafluoroethane
B
1-bromo-1,2,2-trifluoroethene
Conditions | Yield |
---|---|
With bromine trifluoride; bromine In 1,1,1,3,3-pentafluorobutane at -15℃; for 0.25h; |
polytetrafluoroethylene
A
1-bromo-1,2,2-trifluoroethene
B
hexafluoro-1,3-butadiene
Conditions | Yield |
---|---|
Stage #1: polytetrafluoroethylene With magnesium; zinc(II) chloride at 60℃; under 3800.26 Torr; Inert atmosphere; Autoclave; Stage #2: With copper(ll) bromide In benzene-d6 at 20℃; for 0.166667h; Inert atmosphere; Sealed tube; |
1-bromo-1,2,2-trifluoroethene
A
cyclopentadienyl iron(II) dicarbonyl dimer
B
FCF=CFFe(CO)2Cp
Conditions | Yield |
---|---|
With t-butyl alcohol In tetrahydrofuran byproducts: CF2=CFH, t-BuOCF2CFHBr; under Ar; react. in the presence of t-BuOH; alkenyl halide mixed with FpK soln. pre-cooled at -50 °C; after 10-15 min react. mixt. allowed to reach room temp.; not isolated; NMR; | A 95% B 1% |
With PhCH(Et)CN In tetrahydrofuran byproducts: CF2=CFH, CFH=CFC(Et)(Ph)CN, CFHBrCF2C(Et)(Ph)CN; under Ar; react. in the presence of PhCH(Et)CN; alkenyl halide mixed with FpK soln. pre-cooled at -50 °C; after 10-15 min react. mixt. allowed to reach room temp.; not isolated; NMR; | A 77% B 5% |
1-bromo-1,2,2-trifluoroethene
1,1-dibromo-1,2,2,2-tetrafluoroethane
hexafluoro-1,3-butadiene
Conditions | Yield |
---|---|
Stage #1: 1,1-dibromo-1,2,2,2-tetrafluoroethane With aluminum (III) chloride; zinc In 1-methyl-pyrrolidin-2-one at 70 - 90℃; for 3.2h; Inert atmosphere; Stage #2: 1-bromo-1,2,2-trifluoroethene With tetrakis(triphenylphosphine) palladium(0) In 1-methyl-pyrrolidin-2-one at 40℃; for 21.6h; Solvent; Reagent/catalyst; Temperature; Inert atmosphere; | 95% |
ethanol
1-bromo-1,2,2-trifluoroethene
1-ethoxy-1,1,2-trifluoro-2-bromoethane
Conditions | Yield |
---|---|
Stage #1: ethanol With sodium at 20℃; for 0.666667h; Stage #2: 1-bromo-1,2,2-trifluoroethene In ethanol Further stages.; | 93% |
With potassium hydroxide | |
With sodium |
1-bromo-1,2,2-trifluoroethene
2-ethoxycarbonyl-methylisoquinolinium bromide
Conditions | Yield |
---|---|
With potassium carbonate; triethylamine In N,N-dimethyl-formamide at 70℃; for 24h; | 91% |
tetrakis(triethylphosphine)palladium
1-bromo-1,2,2-trifluoroethene
Conditions | Yield |
---|---|
In Petroleum ether (N2); bubbling bromotrifluoroethylene through soln. of (Et3P)4Pd (-196°C); stirring for 10 min; warming to room temp.; removal of solvent in vac.; washing (cold n-hexane); chromy. (florisil,methylene chloride); elem. anal.; | 90% |
decacarbonyldirhenium(0)
1-bromo-1,2,2-trifluoroethene
A
rhenium(I) pentacarbonyl bromide
cis-[CF2=CF(CO)Re(CO)4Br]Na
Conditions | Yield |
---|---|
With Na#Hg In tetrahydrofuran under Ar; soln. of (Re(CO)5)Na (prepd. from Re2(CO)10 and 0.5% NaHg in THF) mixed with alkenyl halide at room temp.; react. completed in less than 4 min; soln. filtered through Celite; THF removed in vacuo; | A 5% B 90% |
1-bromo-1,2,2-trifluoroethene
trimethyltin(IV)chloride
(trifluoro ethylenyl) trimethyl stannane
Conditions | Yield |
---|---|
With hexaethylphosphorous triamide; benzonitrile In benzonitrile under exclusion of moisture; mixt. of Me3SnCl, hexaethylphosphorus triamide, and benzonitrile was degassed at -196°C; CF2CFBr condensed via vacuum; mixt. warmed to 25°C, stirred for 12 h; distd.; | 89% |
triethylsilyl chloride
1-bromo-1,2,2-trifluoroethene
triethyl(trifluorovinyl)silane
Conditions | Yield |
---|---|
With methyllithium In diethyl ether at -78℃; for 4h; | 88% |
1-bromo-1,2,2-trifluoroethene
2-phenacylisoquinolinium bromide
Conditions | Yield |
---|---|
With potassium carbonate; triethylamine In N,N-dimethyl-formamide at 70℃; for 24h; | 86% |
1-bromo-1,2,2-trifluoroethene
2-(4-Bromophenoxy)tetrafluoroethanesulfonyl fluoride
C10H4F8O3S
Conditions | Yield |
---|---|
Stage #1: 1-bromo-1,2,2-trifluoroethene With bromine; zinc; tetrakis(triphenylphosphine) palladium(0) In DMF (N,N-dimethyl-formamide) at 20 - 65℃; for 3.5h; Stage #2: 2-(4-Bromophenoxy)tetrafluoroethanesulfonyl fluoride With tetrakis(triphenylphosphine) palladium(0) In DMF (N,N-dimethyl-formamide) at 75℃; for 10h; | 86% |
1-bromo-1,2,2-trifluoroethene
trifluoroethenylzinc bromide
hexafluoro-1,3-butadiene
Conditions | Yield |
---|---|
With diphenylethoxyphosphine; bis(dibenzylideneacetone)-palladium(0) In N,N-dimethyl-formamide at 20 - 130℃; for 3h; Reagent/catalyst; Temperature; | 85.8% |
With iron(III) chloride at 5℃; Reagent/catalyst; Temperature; Flow reactor; | 80.4% |
2-(trifluoromethyl)-3,3-difluorooxaziridine
1-bromo-1,2,2-trifluoroethene
4-bromo-3-(trifluoromethyl)perfluorooxazolidine
Conditions | Yield |
---|---|
at 55 - 100℃; for 18h; | 85% |
1-bromo-1,2,2-trifluoroethene
bis(fluoroxy)difluoromethane
Conditions | Yield |
---|---|
In Dichlorodifluoromethane at -70℃; for 4h; | 85% |
chloro-trimethyl-silane
1-bromo-1,2,2-trifluoroethene
1,1,2-trifluoro-2-trimethylsilylethylene
Conditions | Yield |
---|---|
With hexaethylphosphoric triamide In benzonitrile for 20h; Ambient temperature; | 85% |
Stage #1: 1-bromo-1,2,2-trifluoroethene With chloro-trimethyl-silane; ethylene dibromide; zinc In N,N-dimethyl-formamide at 20℃; Inert atmosphere; Heating; Stage #2: chloro-trimethyl-silane With copper(l) iodide In N,N-dimethyl-formamide at 20℃; for 4h; Inert atmosphere; Stage #3: With ethylene glycol In N,N-dimethyl-formamide at 20℃; for 1h; Inert atmosphere; | 74% |
With methyllithium In diethyl ether | |
With N,N,N,N-tetraethylammonium tetrafluoroborate In N,N-dimethyl-formamide electrolysis at stainless steel grid cathode and sacrificial zinc anode; | |
With zinc |
1-bromo-1,2,2-trifluoroethene
B
Carbonyl fluoride
C
carbonyl bromide fluoride
D
difluorobromoacetyl fluoride
Conditions | Yield |
---|---|
With oxygen; Nitrogen dioxide at 40.25℃; gas-phase; Further byproducts given; | A n/a B n/a C n/a D 85% |
1-bromo-1,2,2-trifluoroethene
Conditions | Yield |
---|---|
at 450℃; for 0.00555556h; | 85% |
C20H15ClFN3OS
1-bromo-1,2,2-trifluoroethene
5-{5-[4-(2-bromo-1,1,2-trifluoroethoxy)phenyl]-3-methylthiophen-2-yl}-3-(2-chloro-6-fluorophenyl)-1-methyl-1H-[1,2,4]triazole
Conditions | Yield |
---|---|
With sodium hydroxide In N,N-dimethyl-formamide at 25℃; for 1h; | 82% |
1-bromo-1,2,2-trifluoroethene
5-{5-[4-(2-bromo-1,1,2-trifluoroethoxy)phenyl]-3,4-dimethylthiophen-2-yl}-3-(2-chloro-6-fluorophenyl)-1-methyl-1H-[1,2,4]triazole
Conditions | Yield |
---|---|
With sodium hydroxide In N,N-dimethyl-formamide at 25℃; for 1h; | 80% |
1-bromo-1,2,2-trifluoroethene
Conditions | Yield |
---|---|
With potassium carbonate; triethylamine In dimethyl sulfoxide at 70℃; for 18h; | 79% |
Conditions | Yield |
---|---|
In tetrahydrofuran at -196 - 20℃; Schlenk technique; Inert atmosphere; | 79% |
1-bromo-1,2,2-trifluoroethene
perfluoro-NN'-dimethylethane-1,2-bis(amino-oxyl) diradical
Conditions | Yield |
---|---|
under 19 Torr; for 48h; Ambient temperature; | 78% |
Conditions | Yield |
---|---|
With potassium carbonate; triethylamine In N,N-dimethyl-formamide at 70℃; for 24h; | 77% |
1-bromo-1,2,2-trifluoroethene
benzoyl chloride
hexafluoro-2-butyne
2,2,3-trifluoro-4,5-bis(trifluoromethyl)-6-phenyl-2H-pyran
Conditions | Yield |
---|---|
Stage #1: 1-bromo-1,2,2-trifluoroethene With zinc In N,N-dimethyl-formamide Inert atmosphere; Stage #2: With copper(I) bromide In N,N-dimethyl-formamide at 20℃; for 0.25h; Inert atmosphere; Stage #3: benzoyl chloride; hexafluoro-2-butyne stereospecific reaction; Further stages; | 76% |
1-bromo-1,2,2-trifluoroethene
N-(ethoxycarbonylmethyl)pyridinium bromide
Conditions | Yield |
---|---|
With potassium carbonate; triethylamine In N,N-dimethyl-formamide at 70℃; for 24h; | 75% |
1-bromo-1,2,2-trifluoroethene
2-phenacyl-isoquinolinium; chloride
Conditions | Yield |
---|---|
With potassium carbonate; triethylamine In N,N-dimethyl-formamide at 70℃; for 24h; | 74% |
C21H17ClFN3OS
1-bromo-1,2,2-trifluoroethene
5-{4-[4-(2-bromo-1,1,2-trifluoroethoxy)phenyl]-3,5-dimethylthiophen-2-yl}-3-(2-chloro-6-fluorophenyl)-1-methyl-1H-[1,2,4]triazole
Conditions | Yield |
---|---|
With sodium hydroxide In N,N-dimethyl-formamide at 25℃; for 1h; | 74% |
1-bromo-1,2,2-trifluoroethene
Conditions | Yield |
---|---|
With potassium carbonate; triethylamine In dimethyl sulfoxide at 70℃; for 18h; | 72% |
1-bromo-1,2,2-trifluoroethene
copper(I) bromide
zinc
trifluorovinyl copper
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide byproducts: ZnBr2; N2; slight excess of Zn powder added to alkene soln.; mild exothermic reaction after induction period; removal of excess Zn by press. filtrn. under N2; stirring mixt. at 0 °C for half h with CuBr; final warming to room temp.; (19)F NMR; | 72% |
Conditions | Yield |
---|---|
Stage #1: 1-bromo-1,2,2-trifluoroethene With zinc In N,N-dimethyl-formamide Inert atmosphere; Stage #2: With copper(I) bromide In N,N-dimethyl-formamide Inert atmosphere; Stage #3: hexafluoro-2-butyne stereospecific reaction; Further stages; | 72% |
Conditions | Yield |
---|---|
Stage #1: Diphenylacetonitrile With sodium hydride In tetrahydrofuran Stage #2: 1-bromo-1,2,2-trifluoroethene In tetrahydrofuran at 20℃; for 0.5h; | A 15 % Spectr. B 70% |
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