Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H6Cl4 |
| Molecular Weight | 291.988 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC1=CC(Cl)=C(Cl)C(C2=CC=CC=C2)=C1Cl
InChI
InChIKey=BLAYIQLVUNIICD-UHFFFAOYSA-N
InChI=1S/C12H6Cl4/c13-8-6-9(14)12(16)10(11(8)15)7-4-2-1-3-5-7/h1-6H
| Molecular Formula | C12H6Cl4 |
| Molecular Weight | 291.988 |
| 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 |
|
| Solid-phase-microextraction measurement of 62 polychlorinated biphenyl congeners in milliliter sediment pore water samples and determination of K(DOC) values. | 2009-08-15 |
|
| Screening of 397 chemicals and development of a quantitative structure--activity relationship model for androgen receptor antagonism. | 2008-04 |
|
| Dehalococcoides ethenogenes strain 195 reductively dechlorinates diverse chlorinated aromatic pollutants. | 2004-04-01 |
|
| Identification of a microorganism that links its growth to the reductive dechlorination of 2,3,5,6-chlorobiphenyl. | 2001-11 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:58:09 GMT 2025
by
admin
on
Mon Mar 31 18:58:09 GMT 2025
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| Record UNII |
F7XE9G6462
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| Record Status |
Validated (UNII)
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| Record Version |
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C078132
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