Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H9ClO |
| Molecular Weight | 204.652 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC=C(C=C1)C2=CC=C(Cl)C=C2
InChI
InChIKey=ICVFJPSNAUMFCW-UHFFFAOYSA-N
InChI=1S/C12H9ClO/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-8,14H
| Molecular Formula | C12H9ClO |
| Molecular Weight | 204.652 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Hydroxylated metabolites of 4-monochlorobiphenyl and its metabolic pathway in whole poplar plants. | 2010-05-15 |
|
| Direct inhibition of ERK1/2 phosphorylation as a possible mechanism for the antiproliferative action of 3,4-diOH-PCB3 in the MCF-7 cell line. | 2009-10-28 |
|
| 4'-Chloro-biphenyl-4-yl 2,2,2-trichloro-ethyl sulfate. | 2008-11-29 |
|
| Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods. | 2006-11 |
|
| Oxidative ring cleavage of low chlorinated biphenyl derivatives by fungi leads to the formation of chlorinated lactone derivatives. | 2006-07 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:08:34 GMT 2025
by
admin
on
Mon Mar 31 19:08:34 GMT 2025
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| Record UNII |
IN91367N9R
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| Record Status |
Validated (UNII)
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| Record Version |
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28034-99-3
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IN91367N9R
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