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Details

Stereochemistry ACHIRAL
Molecular Formula C6Cl4O2
Molecular Weight 245.875
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of O-CHLORANIL

SMILES

ClC1=C(Cl)C(=O)C(=O)C(Cl)=C1Cl

InChI

InChIKey=VRGCYEIGVVTZCC-UHFFFAOYSA-N
InChI=1S/C6Cl4O2/c7-1-2(8)4(10)6(12)5(11)3(1)9

HIDE SMILES / InChI

Molecular Formula C6Cl4O2
Molecular Weight 245.875
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Proliferation and differentiation of murine haemopoietic progenitor cells in stroma-free culture in the presence of metabolites of chlorinated pesticides.
2001 Feb
Charge-transfer complex formation between o-chloranil and a series of polynuclear aromatic hydrocarbons.
2001 Feb
Inhibition of jack bean urease by tetrachloro-o-benzoquinone and tetrachloro-p-benzoquinone.
2006 Oct
Quantitative analysis of total retronecine esters-type pyrrolizidine alkaloids in plant by high performance liquid chromatography.
2007 Dec 12
Oxidative dimer produced from a 2,3,4-trihydroxybenzoic ester.
2007 Jul
The first structural study on a cyclic tricoordinate phosphorochloridite and a pentacoordinate phosphorane based on 1,2,3,5-protected myo-inositol--a new conformation of 1,3,2-dioxaphosphorinane ring.
2007 Jul 2
Chemical, pulse radiolysis and density functional studies of a new, labile 5,6-indolequinone and its semiquinone.
2007 Mar 2
Synthesis of chromans via [3 + 3] cyclocoupling of phenols with allylic alcohols using a Mo/o-chloranil catalyst system.
2009 Feb 5
Determination of total retronecine esters-type hepatotoxic pyrrolizidine alkaloids in plant materials by pre-column derivatization high-performance liquid chromatography.
2009 Jun
Experimental and theoretical studies of redox reactions of o-chloranil in aqueous solution.
2009 Jun 11
Unexpected formation of a novel pyridinium-containing catecholate ligand and its manganese(III) complex.
2010 Jan 7
In situ coupled oxidation cycle catalyzed by highly active and reusable Pt-catalysts: dehydrogenative oxidation reactions in the presence of a catalytic amount of o-chloranil using molecular oxygen as the terminal oxidant.
2010 Nov 14
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 18:27:38 GMT 2023
Edited
by admin
on Sat Dec 16 18:27:38 GMT 2023
Record UNII
QN2NZL16NG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
O-CHLORANIL
Common Name English
TETRACHLORO-O-BENZOQUINONE
Common Name English
CHLORANIL, O-
Common Name English
NSC-403503
Code English
Code System Code Type Description
EPA CompTox
DTXSID90883844
Created by admin on Sat Dec 16 18:27:39 GMT 2023 , Edited by admin on Sat Dec 16 18:27:39 GMT 2023
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CAS
2435-53-2
Created by admin on Sat Dec 16 18:27:39 GMT 2023 , Edited by admin on Sat Dec 16 18:27:39 GMT 2023
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FDA UNII
QN2NZL16NG
Created by admin on Sat Dec 16 18:27:39 GMT 2023 , Edited by admin on Sat Dec 16 18:27:39 GMT 2023
PRIMARY
NSC
403503
Created by admin on Sat Dec 16 18:27:39 GMT 2023 , Edited by admin on Sat Dec 16 18:27:39 GMT 2023
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PUBCHEM
73252
Created by admin on Sat Dec 16 18:27:39 GMT 2023 , Edited by admin on Sat Dec 16 18:27:39 GMT 2023
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ECHA (EC/EINECS)
219-424-4
Created by admin on Sat Dec 16 18:27:39 GMT 2023 , Edited by admin on Sat Dec 16 18:27:39 GMT 2023
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