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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
Structure of 2,7-DICHLORODIBENZO-P-DIOXIN

SMILES

ClC1=CC2=C(OC3=CC(Cl)=CC=C3O2)C=C1

InChI

InChIKey=NBFMTHWVRBOVPE-UHFFFAOYSA-N
InChI=1S/C12H6Cl2O2/c13-7-1-3-9-11(5-7)16-10-4-2-8(14)6-12(10)15-9/h1-6H

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
Uptake by roots and translocation to shoots of polychlorinated dibenzo-p-dioxins and dibenzofurans in typical crop plants.
2009-08
Influence of soil properties on the biodegradation of 1,3,6,8-tetrachlorodibenzo-p-dioxin and fungal treatment of contaminated paddy soil by white rot fungus Phlebia brevispora.
2009-06
Intron-dependent accumulation of mRNA in Coriolus hirsutus of lignin peroxidase gene the product of which is involved in conversion/degradation of polychlorinated aromatic hydrocarbons.
2006-06
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
Degradation of 2,7-dichlorodibenzo-p-dioxin by Fe(3+)-H(2)O(2) mixed reagent.
2004-11
Trapping of 2,7-dichlorodibenzo-p-dioxin in aqueous solution by enzymatic reaction of fungal manganese peroxidase in the presence of polyunsaturated fatty acids.
2003-09
Degradation of chlorinated biphenyl, dibenzofuran, and dibenzo-p-dioxin by marine bacteria that degrade biphenyl, carbazole, or dibenzofuran.
2003-05
Screening for basidiomycetous fungi capable of degrading 2,7-dichlorodibenzo-p-dioxin.
2002-08-06
Degradation of 2,7-dichlorodibenzo-p-dioxin by wood-rotting fungi, screened by dioxin degrading ability.
2002-07-16
Biodegradation of polychlorinated dibenzo-p-dioxins by recombinant yeast expressing rat CYP1A subfamily.
2002-05-01
Dechlorination of polychlorinated dibenzo-p-dioxins catalyzed by noble metal catalysts under mild conditions.
2002-01
Immunochemical and catalytic characterization of hepatic microsomal cytochrome P450 in the sperm whale (Physeter macrocephalus).
2001-05
Alterations in the growth factor signal transduction pathways and modulators of the cell cycle in endocervical cells from macaques exposed to TCDD.
1998-08
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:50:35 GMT 2025
Edited
by admin
on Mon Mar 31 18:50:35 GMT 2025
Record UNII
3KMT7J3HEQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,7-DICHLORODIBENZO-P-DIOXIN
HSDB  
Common Name English
2,7-DICHLORODIBENZO-P-DIOXIN [HSDB]
Preferred Name English
DIBENZO(B,E)(1,4)DIOXIN, 2,7-DICHLORO-
Systematic Name English
PCDD 11
Common Name English
DICHLORODIBENZO-P-DIOXIN, 2,7-
Common Name English
2,7-DICHLORODIBENZODIOXIN
Systematic Name English
Code System Code Type Description
PUBCHEM
36613
Created by admin on Mon Mar 31 18:50:35 GMT 2025 , Edited by admin on Mon Mar 31 18:50:35 GMT 2025
PRIMARY
MESH
C000925
Created by admin on Mon Mar 31 18:50:35 GMT 2025 , Edited by admin on Mon Mar 31 18:50:35 GMT 2025
PRIMARY
FDA UNII
3KMT7J3HEQ
Created by admin on Mon Mar 31 18:50:35 GMT 2025 , Edited by admin on Mon Mar 31 18:50:35 GMT 2025
PRIMARY
HSDB
4124
Created by admin on Mon Mar 31 18:50:35 GMT 2025 , Edited by admin on Mon Mar 31 18:50:35 GMT 2025
PRIMARY
EPA CompTox
DTXSID1020435
Created by admin on Mon Mar 31 18:50:35 GMT 2025 , Edited by admin on Mon Mar 31 18:50:35 GMT 2025
PRIMARY
CAS
33857-26-0
Created by admin on Mon Mar 31 18:50:35 GMT 2025 , Edited by admin on Mon Mar 31 18:50:35 GMT 2025
PRIMARY