Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H7Cl3 |
| Molecular Weight | 257.543 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC1=CC(=CC=C1)C2=CC(Cl)=CC=C2Cl
InChI
InChIKey=ONNCPBRWFSKDMQ-UHFFFAOYSA-N
InChI=1S/C12H7Cl3/c13-9-3-1-2-8(6-9)11-7-10(14)4-5-12(11)15/h1-7H
| Molecular Formula | C12H7Cl3 |
| Molecular Weight | 257.543 |
| 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 |
|---|---|---|
| Detection and measurement of the agonistic activities of PCBs and mono-hydroxylated PCBs to the constitutive androstane receptor using a recombinant yeast assay. | 2015-10 |
|
| Hydroxylated polychlorinated biphenyls increase reactive oxygen species formation and induce cell death in cultured cerebellar granule cells. | 2009-10-15 |
|
| Screening of 397 chemicals and development of a quantitative structure--activity relationship model for androgen receptor antagonism. | 2008-04 |
|
| Microbial reductive dechlorination of weathered and exogenous co-planar polychlorinated biphenyls (PCBs) in an anaerobic sediment of Venice Lagoon. | 2006-03 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 20:37:54 GMT 2025
by
admin
on
Mon Mar 31 20:37:54 GMT 2025
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| Record UNII |
98H9867N6L
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| Record Status |
Validated (UNII)
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| Record Version |
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34215
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38444-81-4
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98H9867N6L
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38033
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C091160
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DTXSID4074778
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