Details
Stereochemistry | ACHIRAL |
Molecular Formula | C12H5Cl5 |
Molecular Weight | 326.433 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC1=CC(=CC(Cl)=C1)C2=CC(Cl)=C(Cl)C(Cl)=C2
InChI
InChIKey=MXVAYAXIPRGORY-UHFFFAOYSA-N
InChI=1S/C12H5Cl5/c13-8-1-6(2-9(14)5-8)7-3-10(15)12(17)11(16)4-7/h1-5H
Molecular Formula | C12H5Cl5 |
Molecular Weight | 326.433 |
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 Dec |
|
Improved separation of the 209 polychlorinated biphenyl congeners using comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry. | 2004 Jun 25 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:02:27 GMT 2023
by
admin
on
Sat Dec 16 08:02:27 GMT 2023
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Record UNII |
01N0V0N4S2
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Record Status |
Validated (UNII)
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Record Version |
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-
Download
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39635-33-1
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DTXSID9074145
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admin on Sat Dec 16 08:02:27 GMT 2023 , Edited by admin on Sat Dec 16 08:02:27 GMT 2023
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01N0V0N4S2
Created by
admin on Sat Dec 16 08:02:27 GMT 2023 , Edited by admin on Sat Dec 16 08:02:27 GMT 2023
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63085
Created by
admin on Sat Dec 16 08:02:27 GMT 2023 , Edited by admin on Sat Dec 16 08:02:27 GMT 2023
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