Conditions | 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. |
Chemical Name: 1,2-Dibromohexafluoropropane
IUPAC NAME: 1,2-Dibromo-1,1,2,3,3,3-hexafluoropropane
CAS No.: 661-95-0
EINECS: 211-550-8
RTECS: TX8800000
Molecular Formula: C3Br2F6
Molecular Weight: 309.83 g/mol
Density: 2.257 g/cm3
Boiling Point: 72.6 °C at 760 mmHg
Storage temp.: -95 °C
Following is the structure of 1,2-Dibromohexafluoropropane (CAS No.661-95-0):
The chemical synonymous of 1,2-Dibromohexafluoropropane (CAS No.661-95-0) are (+/-)-1,2-Dibromohexafluoropropane ; 1,2-Dibromohexafluoropropane ; 1,2-Dibromo-1,1,2,3,3,3-Hexafluoro-Propan ; 1,2-Dibromo-1,1,2,3,3,3-Hexafluoropropane ; Propane, 1,2-Dibromo-1,1,2,3,3,3-Hexafluoro- ; 1,2-Dibromohexafluoropropane,95% ; 1,2-Dibromohexafluoropropane 98%
1. | orl-rat LDLo:8624 mg/kg | RADLAX Radiology. 105 (1972),323. |
Reported in EPA TSCA Inventory.
Mildly toxic by ingestion. When heated to decomposition it emits toxic vapors of F− and Br−.
Hazard Note: Irritant
Hazard Codes: Xi
Risk Statements about 1,2-Dibromohexafluoropropane (CAS No.661-95-0):
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements about 1,2-Dibromohexafluoropropane (CAS No.661-95-0):
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection.
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