Conditions | Yield |
---|---|
With N-(2-chloro-1,1,2-trifluoroethyl)diethylamine; aluminum (III) chloride; boron trifluoride diethyl etherate In diethyl ether at 20 - 25℃; for 1h; Reagent/catalyst; Temperature; | 87.6% |
With N-(2-chloro-1,1,2-trifluoroethyl)diethylamine; boron trifluoride diethyl etherate In diethyl ether at 20 - 70℃; under 1 - 3 Torr; for 1h; Reagent/catalyst; Solvent; Temperature; Inert atmosphere; | 87.6% |
1,2,5,6-diepoxyperfluorohexane
perfluorosuccinic difluoride
Conditions | Yield |
---|---|
at 210 - 220℃; for 6h; | 85% |
perfluorosuccinic difluoride
Conditions | Yield |
---|---|
With potassium fluoride at 100℃; for 5h; Large scale; | 85% |
With potassium fluoride at 100℃; for 5h; | 85% |
Conditions | Yield |
---|---|
Electrochemical reaction; | 83% |
perfluorosuccinic difluoride
Conditions | Yield |
---|---|
With sulfur tetrafluoride at 150℃; for 5h; | 81% |
Perfluoro-1,5-hexadiene
A
perfluorosuccinic difluoride
B
1,2,5,6-diepoxyperfluorohexane
C
2,2,3,3-Tetrafluoro-3-(2,3,3-trifluoro-oxiranyl)-propionyl fluoride
Conditions | Yield |
---|---|
With air for 32h; Irradiation; | A n/a B 65% C n/a |
With air for 32h; Irradiation; | A n/a B n/a C 27% |
1,1,2,2,3,3,4,4-octafluoro-1,4-diiodobutane
A
hexafluoro-dihydro-furan-2-one
B
perfluorosuccinic difluoride
Conditions | Yield |
---|---|
With sulfur trioxide | A 7% B n/a |
Conditions | Yield |
---|---|
With sodium fluoride |
1,4-bis(fluorosulfonyloxy)octafluorobutane
perfluorosuccinic difluoride
Conditions | Yield |
---|---|
With potassium fluoride In diethylene glycol dimethyl ether | |
With cesium fluoride at 50℃; |
Perfluoro-1,5-hexadiene
A
1,2-epoxyperfluoro-5-hexene
B
perfluorosuccinic difluoride
C
1,2,5,6-diepoxyperfluorohexane
D
2,2,3,3-Tetrafluoro-3-(2,3,3-trifluoro-oxiranyl)-propionyl fluoride
Conditions | Yield |
---|---|
With air at 25℃; Product distribution; Irradiation; var. time; |
Conditions | Yield |
---|---|
With sodium fluoride at 100℃; for 0.25h; | A n/a B 52 % Spectr. |
Conditions | Yield |
---|---|
With fluorine at 180℃; for 4h; |
perfluorosuccinic difluoride
Conditions | Yield |
---|---|
With lithium iodide at 120℃; for 3.5h; | A 1% B 96% |
With lithium iodide at 120℃; for 5h; | A 55% B 7% |
perfluorosuccinic difluoride
Conditions | Yield |
---|---|
With lithium bromide at 250℃; for 5h; | A 1% B 88% |
With lithium bromide at 250℃; for 5h; | A 56% B 19% |
perfluorosuccinic difluoride
2-Isopropylimino-2-phenylethane
Conditions | Yield |
---|---|
In diethyl ether at 0℃; for 12h; Acylation; | 88% |
Conditions | Yield |
---|---|
With lithium chloride at 330℃; for 5h; | A 80% B 8% |
With lithium chloride at 330℃; for 5h; | A 25% B 71% |
Conditions | Yield |
---|---|
In cyclohexane at 0℃; for 12h; Acylation; Stork reaction; Cyclization; | 80% |
perfluoropropylene
perfluorosuccinic difluoride
2H,7H-dodecafluoro-2,7-bis-trifluoromethyl-octane-3,6-dione
Conditions | Yield |
---|---|
With potassium fluoride In diethylene glycol dimethyl ether at 70 - 80℃; under 22.8015 Torr; for 5 - 20h; Product distribution / selectivity; Cooling with acetone-dry ice; | 78% |
With potassium fluoride In benzonitrile |
perfluorosuccinic difluoride
2-Isopropylimino-2-phenylethane
Conditions | Yield |
---|---|
In chloroform at 30℃; for 12h; Acylation; Stork reaction; Cyclization; | 75% |
perfluorosuccinic difluoride
2-Isopropylimino-2-phenylethane
Conditions | Yield |
---|---|
In diethyl ether at 0℃; for 12h; Acylation; Stork reaction; Cyclization; | A n/a B 67% |
Hexafluoropropene oxide
perfluorosuccinic difluoride
perfluoro-2-methyl-3-oxaheptanedioyl fluoride
Conditions | Yield |
---|---|
With cesium fluoride at -10℃; Autoclave; | 62% |
With cesium fluoride Autoclave; | 62% |
With potassium fluoride In diethylene glycol dimethyl ether |
perfluorosuccinic difluoride
benzene
2,2,3,3-tetrafluoro-1,4-diphenylbutane-1,4-dione
Conditions | Yield |
---|---|
With aluminium trichloride Heating; | 60% |
Conditions | Yield |
---|---|
Stage #1: perfluorosuccinic difluoride With sodium tetrahydroborate In isopropyl alcohol at 5 - 80℃; for 3h; Stage #2: With sulfuric acid In isopropyl alcohol at 35℃; for 1h; | 53% |
perfluorosuccinic difluoride
Conditions | Yield |
---|---|
With lithium bromide; lithium iodide at 120℃; for 20h; Yields of byproduct given; | A n/a B 49% C n/a |
Conditions | Yield |
---|---|
With lithium chloride; lithium bromide at 250℃; for 24h; Yields of byproduct given; | A n/a B 46% C n/a |
Conditions | Yield |
---|---|
With lithium chloride; lithium iodide at 80℃; for 90h; Further byproducts given. Yields of byproduct given; | A n/a B n/a C 41% D n/a |
Conditions | Yield |
---|---|
In diethyl ether at 0℃; for 12h; Acylation; Stork reaction; Cyclization; | A n/a B 40% |
perfluoropropylene
perfluorosuccinic difluoride
Perfluor-5-methyl-4-keto-hexansaeurefluorid
Conditions | Yield |
---|---|
With potassium fluoride In benzonitrile |
perfluorosuccinic difluoride
Octafluor-1,4-bis(fluoroxy)butan
Conditions | Yield |
---|---|
With fluorine; cesium fluoride |
perfluorosuccinic difluoride
A
1,2-dibromo-1,1,2,2-tetrafluoroethane
B
tetrafluorosuccinyl chloride
C
3-bromo-2,2,3,3-tetrafluoropropanoyl chloride
Conditions | Yield |
---|---|
With lithium chloride; lithium bromide at 350℃; for 5h; Yield given. Yields of byproduct given; |
perfluorosuccinic difluoride
A
1,2-diiodotetrafluoroethane
B
tetrafluorosuccinyl chloride
C
2,2,3,3-Tetrafluoro-3-iodo-propionyl fluoride
Conditions | Yield |
---|---|
With lithium chloride; lithium iodide at 230℃; for 5.5h; Yield given. Further byproducts given. Yields of byproduct given; |
Conditions | Yield |
---|---|
With ammonia |
The CAS register number of Butanedioyl difluoride,2,2,3,3-tetrafluoro- is 679-13-0. It also can be called as Perfluorosuccinic difluoride and the systematic name about this chemical is tetrafluorobutanedioyl difluoride. The molecular formula about this chemical is C4F6O2 and the molecular weight is 194.03.
Physical properties about Butanedioyl difluoride,2,2,3,3-tetrafluoro- are: (1)ACD/LogP: 4.42; (2)ACD/LogD (pH 5.5): 4.42; (3)ACD/LogD (pH 7.4): 4.42; (4)ACD/BCF (pH 5.5): 1355.23; (5)ACD/BCF (pH 7.4): 1355.23; (6)ACD/KOC (pH 5.5): 6074.27; (7)ACD/KOC (pH 7.4): 6074.27; (8)#H bond acceptors: 2; (9)#Freely Rotating Bonds: 3; (10)Polar Surface Area: 34.14 Å2; (11)Index of Refraction: 1.283; (12)Molar Refractivity: 21.55 cm3; (13)Molar Volume: 121.5 cm3; (14)Polarizability: 8.54x10-24cm3; (15)Surface Tension: 17.4 dyne/cm; (16)Density: 1.595 g/cm3; (17)Flash Point: 26.1 °C; (18)Enthalpy of Vaporization: 33.38 kJ/mol; (19)Boiling Point: 94.1 °C at 760 mmHg; (20)Vapour Pressure: 48.1 mmHg at 25 °C.
When you are using this chemical, please be cautious about it as the following:
This chemical can cause burns. If you want to use this chemical, wear suitable protective clothing and gloves. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
You can still convert the following datas into molecular structure:
(1)SMILES: FC(F)(C(F)=O)C(F)(F)C(F)=O
(2)InChI: InChI=1/C4F6O2/c5-1(11)3(7,8)4(9,10)2(6)12
(3)InChIKey: KNURRSZDMIXZLO-UHFFFAOYAL
(4)Std. InChI: InChI=1S/C4F6O2/c5-1(11)3(7,8)4(9,10)2(6)12
(5)Std. InChIKey: KNURRSZDMIXZLO-UHFFFAOYSA-N
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