Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H6Cl2O2 |
| Molecular Weight | 253.081 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC1=C(Cl)C2=C(OC3=CC=CC=C3O2)C=C1
InChI
InChIKey=DFGDMWHUCCHXIF-UHFFFAOYSA-N
InChI=1S/C12H6Cl2O2/c13-7-5-6-10-12(11(7)14)16-9-4-2-1-3-8(9)15-10/h1-6H
| Molecular Formula | C12H6Cl2O2 |
| Molecular Weight | 253.081 |
| 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 |
|---|---|---|
| Further research on the photo-SPME of triclosan. | 2006-04 |
|
| Rat cytochrome P450-mediated transformation of dichlorodibenzo-p-dioxins by recombinant white-rot basidiomycete Coriolus hirsutus. | 2005-11 |
|
| Biotransformation of dichloro-, trichloro-, and tetrachlorodibenzo-p-dioxin by the white-rot fungus Phlebia lindtneri. | 2005-09 |
|
| Confirmation of the formation of dichlorodibenzo-p-dioxin in the photodegradation of triclosan by photo-SPME. | 2005-03 |
|
| Temperature dependence of DCDD/F isomer distributions from chlorophenol precursors. | 2001-02-24 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:57:47 GMT 2025
by
admin
on
Mon Mar 31 21:57:47 GMT 2025
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| Record UNII |
QEQ8K3CG9Q
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| Record Status |
Validated (UNII)
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| Record Version |
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