Details
Stereochemistry | ACHIRAL |
Molecular Formula | C12H8Cl2 |
Molecular Weight | 223.098 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC1=CC=C(C=C1)C2=C(Cl)C=CC=C2
InChI
InChIKey=UFNIBRDIUNVOMX-UHFFFAOYSA-N
InChI=1S/C12H8Cl2/c13-10-7-5-9(6-8-10)11-3-1-2-4-12(11)14/h1-8H
Molecular Formula | C12H8Cl2 |
Molecular Weight | 223.098 |
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 |
---|---|---|
Sorption of 2,4'-dichlorobiphenyl and fluoranthene to a marine sediment amended with different types of black carbon. | 2004 Nov |
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Retention indexes for temperature-programmed gas chromatography of polychlorinated biphenyls. | 2004 Sep 15 |
|
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods. | 2006 Nov |
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Screening of 397 chemicals and development of a quantitative structure--activity relationship model for androgen receptor antagonism. | 2008 Apr |
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Binding interactions of hydroxylated polychlorinated biphenyls (OHPCBs) with human hydroxysteroid sulfotransferase hSULT2A1. | 2014 Apr 5 |
|
Detection and measurement of the agonistic activities of PCBs and mono-hydroxylated PCBs to the constitutive androstane receptor using a recombinant yeast assay. | 2015 Oct |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:58:37 GMT 2023
by
admin
on
Sat Dec 16 10:58:37 GMT 2023
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Record UNII |
TTP086070W
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Record Status |
Validated (UNII)
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Record Version |
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