Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C2H2ClF3 |
| Molecular Weight | 118.485 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
FC(F)(F)CCl
InChI
InChIKey=CYXIKYKBLDZZNW-UHFFFAOYSA-N
InChI=1S/C2H2ClF3/c3-1-2(4,5)6/h1H2
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| 1-Chloro-2,2,2-trifluoroethyl radical: Formation from halothane by human cytochrome P-450 in reconstituted vesicles and binding to phospholipids. | 1981 Sep 16 |
|
| Reductive metabolism of halothane by human and rabbit cytochrome P-450. Binding of 1-chloro-2,2,2-trifluoroethyl radical to phospholipids. | 1982 May |
|
| Production of 5- and 15-hydroperoxyeicosatetraenoic acid from arachidonic acid by halothane-free radicals generated by UV-irradiation. | 1984 Mar |
|
| Halothane-dependent lipid peroxidation in human liver microsomes is catalyzed by cytochrome P4502A6 (CYP2A6). | 2001 Aug |
Patents
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| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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IARC | 2-Chloro-1,1,1-trifluoroethane |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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6408
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DTXSID5020289
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200-912-0
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6949
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H86O899T9B
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1,1,1-Trifluoro-2-chloroethane
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75-88-7
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PARENT (METABOLITE)
SUBSTANCE RECORD
