Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C3H3Cl3O |
| Molecular Weight | 161.414 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC(Cl)(Cl)C1CO1
InChI
InChIKey=VFEXYZINKMLLAK-UHFFFAOYSA-N
InChI=1S/C3H3Cl3O/c4-3(5,6)2-1-7-2/h2H,1H2
| Molecular Formula | C3H3Cl3O |
| Molecular Weight | 161.414 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Microsomal biotransformation of benzo[ghi]perylene, a mutagenic polycyclic aromatic hydrocarbon without a "classic" bay region. | 2005-04 |
|
| The metabolism of beta-chloroprene: preliminary in-vitro studies using liver microsomes. | 2001-06-01 |
|
| Stereoselective epoxidation and hydration at the K-region of polycyclic aromatic hydrocarbons by cDNA-expressed cytochromes P450 1A1, 1A2, and epoxide hydrolase. | 1996-12-10 |
|
| Influence of modulators of epoxide metabolism on the cytotoxicity of trans-anethole in freshly isolated rat hepatocytes. | 1992-06 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:02:13 GMT 2025
by
admin
on
Mon Mar 31 22:02:13 GMT 2025
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| Record UNII |
IQ92Z3552X
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| Record Status |
Validated (UNII)
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