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inquiryfactory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
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inquiry1, High quality with competitive price:2, Fast and safe delivery3.Excellent pre-sales and after-sales service4. Well-trained and professional technologist and sales with rich experience in the field for 5-10 yearsAppearance:see detailed specification
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inquiryLower price, sample is available,SDS test documents are available,large stock in warehouseAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:Fine chemical intermediates, used as the main raw material for the synthe
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inquiry1,2-Dibromohexafluoropropane CAS:661-95-0 from FandaChem Appearance:as in COA Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express Port:Shanghai, China
Cas:661-95-0
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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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inquiryWe product this chemical more than 10 years . We are very experience to export it to many countries, Our superior & stable quality , competitive price gain warm reception from our customers. Application:Chemical intermediate
1,2-Dibromohexafluoropropane Application:1,2-Dibromohexafluoropropane
Factory supply high purity low priceAppearance:solid or liquid Storage:sealed in cool and dry place Package:As customer's requested Application:Pharma Intermediate Transportation:by courier/air/sea Port:Any port in China
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inquiryfactory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
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inquiry1,2-DibromohexafluoropropaneAppearance:white powder Storage:Shading, sealed, dry place. Package:aluminous bag Application:API Transportation:By express (Door to door) such as FEDEX, DHL, EMS for small amount. By air(airport to airport) or by sea LCL/
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inquiryConditions | Yield |
---|---|
With bromine at 100℃; Cooling with acetone-dry ice; | 99.41% |
With bromine at 20℃; for 19h; | 95% |
With bromine for 19h; | 95% |
perfluoropropylene
Bromine(I) trifluoromethanesulfonate
A
1,2-dibromohexafluoropropane
B
trifluoromethyl trifluoromethanesulfonate
C
Trifluoro-methanesulfonic acid 2-bromo-1,1,2,3,3,3-hexafluoro-propyl ester
Conditions | Yield |
---|---|
at -111 - -5℃; for 24h; | A n/a B n/a C 80% |
1,1,1,3,3,3-hexafluoropropane
A
1,2-dibromohexafluoropropane
B
1,1,1,3,3,3-hexafluoroisopropyl bromide
Conditions | Yield |
---|---|
With bromine at 600℃; |
HFC-227ca
A
bromodifluoromethane
B
1,2-dibromohexafluoropropane
C
Bromotrifluoromethane
D
dibromodifluoromethane
E
1-bromo-1,1,2,2-tetrafluoro-ethane
F
bromopentafluoroethane
Conditions | Yield |
---|---|
With bromine under 0.05 Torr; Rate constant; Product distribution; Irradiation; Infrared multiphoton dissociation with Br2 as a scavenger.; |
perfluoropropylene
A
1,2-dibromohexafluoropropane
B
2-bromo-1,1,1,2,3,3,3-heptafluoropropane
C
2-bromohexafluoropropyl fluorosulfate
D
2-hydrohexafluoropropyl fluorosulfate
Conditions | Yield |
---|---|
With bromine; antimony pentafluoride; fluorosulphonic acid for 48h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
heptafluorobutyric Acid
bromine
A
1,2-dibromohexafluoropropane
B
perfluoropropyl bromide
Conditions | Yield |
---|---|
at 260℃; Reaktion des Natrium-Salzes; |
1,1,1,3,3,3-hexafluoropropane
bromine
A
1,2-dibromohexafluoropropane
B
1,1,1,3,3,3-hexafluoroisopropyl bromide
Conditions | Yield |
---|---|
at 600℃; |
Conditions | Yield |
---|---|
With potassium carbonate |
1,2-dibromohexafluoropropane
2,2-dibromo-1,1,1,3,3,3-hexafluoropropane
Conditions | Yield |
---|---|
With ACF In chloroform-d1 at 25℃; for 2h; Reagent/catalyst; | 100% |
aluminium trichloride In N,N-dimethyl-formamide at 150℃; for 120h; | 72% |
With aluminium trichloride at 150℃; for 216h; | 67% |
Conditions | Yield |
---|---|
With sulfolane; potassium fluoride at 120 - 175℃; under 2250.23 - 10126 Torr; for 6h; | 95.8% |
With sulfolane; potassium fluoride at 125 - 175℃; under 2250.23 - 10126 Torr; for 5h; | 83% |
With potassium fluoride In N,N-dimethyl-formamide at 90 - 140℃; for 3h; | |
With sulfolane; potassium fluoride at 125℃; for 27h; Autoclave; Inert atmosphere; |
1,2-dibromohexafluoropropane
1,7-Octadiene
(cis/trans)-1-Bromomethyl-2-(3-bromo-2-trifluoromethyl-2,3,3-trifluoropropyl)cyclohexane
Conditions | Yield |
---|---|
With bis(cyclopentadienyl)titanium dichloride; iron In ethanol at 60℃; for 13h; | 88% |
1,2-dibromohexafluoropropane
potassium phenolate
A
1-phenoxy-2-hydroperfluoropropane
B
(2-Bromo-1,1,2,3,3,3-hexafluoro-propoxy)-benzene
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide for 8h; Ambient temperature; | A 2% B 80% |
Conditions | Yield |
---|---|
With sodium thiosulfate; sodium hydrogencarbonate; tetra(n-butyl)ammonium hydrogensulfate In tert-butyl methyl ether; water at 20 - 40℃; | 65% |
With sodium dithionite; tetra(n-butyl)ammonium hydrogensulfate; sodium hydrogencarbonate In tert-butyl methyl ether; water for 3h; | 33% |
1,2-dibromohexafluoropropane
A
1-bromo-1,1,2,3,3,3-hexafluoro-propane
B
perfluoropropylene
C
1,1,1,2,3,3-hexafluoropropane
D
2-bromo-1,1,1,2,3,3-hexafluoro-propane
Conditions | Yield |
---|---|
With tri-n-butyl-tin hydride for 1.5h; Product distribution; Heating; | A 53% B 3% C 14% D 21% |
1,2-dibromohexafluoropropane
o-toluidine
4-[1-(bromo-difluoro-methyl)-1,2,2,2-tetrafluoro-ethyl]-2-methyl-phenylamine
Conditions | Yield |
---|---|
With sodium thiosulfate; sodium hydrogencarbonate; tetra(n-butyl)ammonium hydrogensulfate In tert-butyl methyl ether; water at 20 - 40℃; for 18h; | 53% |
piperidine
1,2-dibromohexafluoropropane
A
1-(1,1,2,3,3,3-hexafluoro-propyl)-piperidine
B
1-pentafluoropropenyl-piperidine
C
1-(2,3,3,3-tetrafluoro-propionyl)-piperidine
D
1-(2-Bromo-1,1,2,3,3,3-hexafluoro-propyl)-piperidine
Conditions | Yield |
---|---|
With sodium hydride; triethylamine In N,N-dimethyl-formamide at -5℃; for 6h; | A 1 % Spectr. B 20% C n/a D 33% |
1,2-dibromohexafluoropropane
diethylamine
A
hexafluoropropene-diethylamine adduct
B
diethyl-(pentafluoro-propenyl)-amine
C
(2-Bromo-1,1,2,3,3,3-hexafluoro-propyl)-diethyl-amine
Conditions | Yield |
---|---|
With sodium hydride; triethylamine In N,N-dimethyl-formamide at -5℃; for 6h; | A 1 % Spectr. B 21% C 32% |
With n-butyllithium; triethylamine In N,N-dimethyl-formamide at -5℃; for 6h; Product distribution; various temperatures, time, and reagents; | A 1 % Spectr. B 20 % Spectr. C 65 % Spectr. |
1,2-dibromohexafluoropropane
2-(difluoromethoxy)aniline
4-(1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl)-6-(difluoromethoxy)aniline
Conditions | Yield |
---|---|
With sodium dithionite; tetra(n-butyl)ammonium hydrogensulfate; sodium hydrogencarbonate In tert-butyl methyl ether; water at 18 - 30℃; for 48h; | 26% |
pyrrolidine
1,2-dibromohexafluoropropane
A
1-(1,1,2,3,3,3-hexafluoro-propyl)-pyrrolidine
B
1-(2-Bromo-1,1,2,3,3,3-hexafluoro-propyl)-pyrrolidine
C
1-((E)-Pentafluoro-propenyl)-pyrrolidine
D
2,3,3,3-Tetrafluoro-1-pyrrolidin-1-yl-propan-1-one
Conditions | Yield |
---|---|
With sodium hydride; triethylamine In N,N-dimethyl-formamide at -5℃; for 6h; | A 1 % Spectr. B 21% C 15 % Spectr. D n/a |
Conditions | Yield |
---|---|
With sodium thiosulfate; sodium hydrogencarbonate; tetra(n-butyl)ammonium hydrogensulfate In tert-butyl methyl ether; water at 20 - 40℃; for 12h; | 14% |
1,2-dibromohexafluoropropane
perfluoropropylene
1,4-dibromo-nonafluoro-2-trifluoromethyl-pentane
Conditions | Yield |
---|---|
at 255℃; under 213297 Torr; |
1,2-dibromohexafluoropropane
perfluoropropylene
1,6-dibromo-dodecafluoro-2,4-bis-trifluoromethyl-heptane
Conditions | Yield |
---|---|
at 250℃; |
Conditions | Yield |
---|---|
With acetic acid; zinc at 25℃; | |
With ethanol; zinc |
1,2-dibromohexafluoropropane
ethene
1,4-dibromo-1,1,2-trifluoro-2-(trifluoromethyl)butane
Conditions | Yield |
---|---|
With dibenzoyl peroxide |
pyrrolidine
1,2-dibromohexafluoropropane
A
1-(1,1,2,3,3,3-hexafluoro-propyl)-pyrrolidine
B
1-(2-Bromo-1,1,2,3,3,3-hexafluoro-propyl)-pyrrolidine
C
1-((E)-Pentafluoro-propenyl)-pyrrolidine
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl-formamide at 40℃; for 20h; | A 15 % Spectr. B 13 % Spectr. C 1 % Spectr. |
1,2-dibromohexafluoropropane
perfluoroisobutylene
A
2-bromo-1,1,1,3,3,3-hexafluoro-2-trifluoromethyl-propane
B
Perfluoro-4,4-dimethylpent-2-ene
Conditions | Yield |
---|---|
With cesium fluoride In diethylene glycol dimethyl ether for 2.5h; Product distribution; various vicinal dihalopolyfluoroalkanes; |
Conditions | Yield |
---|---|
With N,N,N,N,N,N-hexamethylphosphoric triamide; sodium azide at 80℃; for 27h; Yield given. Yields of byproduct given; |
1,2-dibromohexafluoropropane
diethylamine
A
hexafluoropropene-diethylamine adduct
B
diethyl-(pentafluoro-propenyl)-amine
C
N,N'-diethyl-1,2,2,2-tetrafluoropropionamide
D
(2-Bromo-1,1,2,3,3,3-hexafluoro-propyl)-diethyl-amine
Conditions | Yield |
---|---|
With n-butyllithium; triethylamine In N,N-dimethyl-formamide at -5℃; for 2h; | A 1 % Spectr. B 20 % Spectr. C n/a D 65 % Spectr. |
1,2-dibromohexafluoropropane
allyl-trimethyl-silane
5-Bromo-4,5,5-trifluoro-4-trifluoromethyl-pent-1-ene
Conditions | Yield |
---|---|
With ethanolamine; triiron dodecarbonyl at 60℃; for 20h; sealed tube; | 40 % Chromat. |
1,2-dibromohexafluoropropane
ethenyltrimethylsilane
(1,4-Dibromo-3,4,4-trifluoro-3-trifluoromethyl-butyl)-trimethyl-silane
Conditions | Yield |
---|---|
With ethanolamine; triiron dodecarbonyl at 60℃; for 20h; | 38 % Chromat. |
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