Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H5Cl5O |
| Molecular Weight | 342.433 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC=C(C=C1Cl)C2=C(Cl)C=C(Cl)C(Cl)=C2Cl
InChI
InChIKey=QLPPOBFMEBKBOZ-UHFFFAOYSA-N
InChI=1S/C12H5Cl5O/c13-6-3-5(1-2-9(6)18)10-7(14)4-8(15)11(16)12(10)17/h1-4,18H
| Molecular Formula | C12H5Cl5O |
| Molecular Weight | 342.433 |
| 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 polychlorinated biphenyls selectively bind transthyretin in blood and inhibit amyloidogenesis: rationalizing rodent PCB toxicity. | 2004-12 |
|
| Potent inhibition of estrogen sulfotransferase by hydroxylated PCB metabolites: a novel pathway explaining the estrogenic activity of PCBs. | 2000-05 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 20:37:50 GMT 2025
by
admin
on
Mon Mar 31 20:37:50 GMT 2025
|
| Record UNII |
5WCD5150FG
|
| Record Status |
Validated (UNII)
|
| Record Version |
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5WCD5150FG
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DTXSID20172793
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644181
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admin on Mon Mar 31 20:37:50 GMT 2025 , Edited by admin on Mon Mar 31 20:37:50 GMT 2025
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192190-10-6
Created by
admin on Mon Mar 31 20:37:50 GMT 2025 , Edited by admin on Mon Mar 31 20:37:50 GMT 2025
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