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Details

Stereochemistry ACHIRAL
Molecular Formula C12H8Cl2
Molecular Weight 223.098
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,2'-DICHLOROBIPHENYL

SMILES

ClC1=CC=CC=C1C2=CC=CC=C2Cl

InChI

InChIKey=JAYCNKDKIKZTAF-UHFFFAOYSA-N
InChI=1S/C12H8Cl2/c13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)14/h1-8H

HIDE SMILES / InChI

Molecular Formula C12H8Cl2
Molecular Weight 223.098
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Evidence for unique and ubiquitous environmental sources of 3,3'-dichlorobiphenyl (PCB 11).
2010-04-15
Screening of 397 chemicals and development of a quantitative structure--activity relationship model for androgen receptor antagonism.
2008-04
Peroxidase-mediated removal of a polychlorinated biphenyl using natural organic matter as the sole cosubstrate.
2007-02-01
A comparison of two techniques for studying sediment desorption kinetics of hydrophobic pollutants.
2007-01
Dinuclear gold(I) isocyanide complexes with luminescent properties, and displaying thermotropic liquid crystalline behavior.
2006-12-11
Potential role for oxidative stress in 2,2'-dichlorobiphenyl-induced inhibition of uterine contractions but not myometrial gap junctions.
2006-09
Oxidative ring cleavage of low chlorinated biphenyl derivatives by fungi leads to the formation of chlorinated lactone derivatives.
2006-07
Active-site engineering of biphenyl dioxygenase: effect of substituted amino acids on substrate specificity and regiospecificity.
2006-06
2,2'-Dichlorobiphenyl decreases amplitude and synchronization of uterine contractions through MAPK1-mediated phosphorylation of GJA1 (connexin43) and inhibition of myometrial gap junctions.
2005-11
Revisiting the regiospecificity of Burkholderia xenovorans LB400 biphenyl dioxygenase toward 2,2'-dichlorobiphenyl and 2,3,2',3'-tetrachlorobiphenyl.
2004-11-12
Evolution of the biphenyl dioxygenase BphA from Burkholderia xenovorans LB400 by random mutagenesis of multiple sites in region III.
2004-11-12
Effect of sorbate planarity on environmental black carbon sorption.
2004-07-01
Mechanochemical removal of organo-chlorinated compounds by inorganic components of soil.
2004-06
Vesicular catecholamine release from rat PC12 cells on acute and subchronic exposure to polychlorinated biphenyls.
2002-09-15
Foci formation of MCF7 cells as an in vitro screening method for estrogenic chemicals.
2002-03
Dechlorination of polychlorobiphenyls using NaBH(4) and NaBH(4)/LiCl at 120-310 degrees C in glyme solvents.
2001-04-20
Possible molecular targets of halogenated aromatic hydrocarbons in neuronal cells.
2001-02-09
Substance Class Chemical
Created
by admin
on Mon Mar 31 23:32:57 GMT 2025
Edited
by admin
on Mon Mar 31 23:32:57 GMT 2025
Record UNII
1433W7U14D
Record Status Validated (UNII)
Record Version
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Name Type Language
2,2'-DICHLOROBIPHENYL
Systematic Name English
NSC-59902
Preferred Name English
PCB 4
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID4044533
Created by admin on Mon Mar 31 23:32:57 GMT 2025 , Edited by admin on Mon Mar 31 23:32:57 GMT 2025
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NSC
59902
Created by admin on Mon Mar 31 23:32:57 GMT 2025 , Edited by admin on Mon Mar 31 23:32:57 GMT 2025
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PUBCHEM
25622
Created by admin on Mon Mar 31 23:32:57 GMT 2025 , Edited by admin on Mon Mar 31 23:32:57 GMT 2025
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CAS
13029-08-8
Created by admin on Mon Mar 31 23:32:57 GMT 2025 , Edited by admin on Mon Mar 31 23:32:57 GMT 2025
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FDA UNII
1433W7U14D
Created by admin on Mon Mar 31 23:32:57 GMT 2025 , Edited by admin on Mon Mar 31 23:32:57 GMT 2025
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