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
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
| 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
| Title | Date | PubMed |
|---|---|---|
| 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. | 2010-11-14 |
|
| Unexpected formation of a novel pyridinium-containing catecholate ligand and its manganese(III) complex. | 2010-01-07 |
|
| Experimental and theoretical studies of redox reactions of o-chloranil in aqueous solution. | 2009-06-11 |
|
| Determination of total retronecine esters-type hepatotoxic pyrrolizidine alkaloids in plant materials by pre-column derivatization high-performance liquid chromatography. | 2009-06 |
|
| Synthesis of chromans via [3 + 3] cyclocoupling of phenols with allylic alcohols using a Mo/o-chloranil catalyst system. | 2009-02-05 |
|
| Determination of individual proton affinities of reserpine from its UV-vis and charge-transfer spectra. | 2008-07-31 |
|
| Versatile Friedel-Crafts-type alkylation of benzene derivatives using a molybdenum complex/ortho-chloranil catalytic system. | 2008 |
|
| Quantitative analysis of total retronecine esters-type pyrrolizidine alkaloids in plant by high performance liquid chromatography. | 2007-12-12 |
|
| 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. | 2007-07-02 |
|
| Oxidative dimer produced from a 2,3,4-trihydroxybenzoic ester. | 2007-07 |
|
| Chemical, pulse radiolysis and density functional studies of a new, labile 5,6-indolequinone and its semiquinone. | 2007-03-02 |
|
| Inhibition of jack bean urease by tetrachloro-o-benzoquinone and tetrachloro-p-benzoquinone. | 2006-10 |
|
| Electronic structures of intermolecular charge-transfer states in fast electron transfers with tetrathiafulvalene donor. Thermal and photoactivation of [2 + 4] cycloaddition to o-chloranil acceptor. | 2006-10 |
|
| Spectrophotometric and electrical studies of charge transfer complexes of 2-amino-1,3,4-thiadiazole with pi-acceptors. | 2005-11 |
|
| Spectroscopic and thermodynamic study of charge transfer complexes of cloxacillin sodium in aqueous ethanol medium. | 2005-07 |
|
| The effect of pressure on hydrogen transfer reactions with quinones. | 2004-06-07 |
|
| Formation and removal of pentachlorophenol-derived protein adducts in rodent liver under acute, multiple, and chronic dosing regimens. | 2003-05 |
|
| Vertical ionisation potentials of a number of crown ethers from charge transfer bands of their EDA complexes. | 2002-11 |
|
| Spectrophotometric study of molecular complex formation between o-chloranil and a series of methylated pyridines. | 2002-05 |
|
| Room temperature solution studies of complexation between o-chloranil and a series of anilines by spectrophotometric method. | 2001-10 |
|
| Proliferation and differentiation of murine haemopoietic progenitor cells in stroma-free culture in the presence of metabolites of chlorinated pesticides. | 2001-02 |
|
| Charge-transfer complex formation between o-chloranil and a series of polynuclear aromatic hydrocarbons. | 2001-02 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 11:13:04 GMT 2025
by
admin
on
Wed Apr 02 11:13:04 GMT 2025
|
| Record UNII |
QN2NZL16NG
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DTXSID90883844
Created by
admin on Wed Apr 02 11:13:04 GMT 2025 , Edited by admin on Wed Apr 02 11:13:04 GMT 2025
|
PRIMARY | |||
|
2435-53-2
Created by
admin on Wed Apr 02 11:13:04 GMT 2025 , Edited by admin on Wed Apr 02 11:13:04 GMT 2025
|
PRIMARY | |||
|
QN2NZL16NG
Created by
admin on Wed Apr 02 11:13:04 GMT 2025 , Edited by admin on Wed Apr 02 11:13:04 GMT 2025
|
PRIMARY | |||
|
403503
Created by
admin on Wed Apr 02 11:13:04 GMT 2025 , Edited by admin on Wed Apr 02 11:13:04 GMT 2025
|
PRIMARY | |||
|
73252
Created by
admin on Wed Apr 02 11:13:04 GMT 2025 , Edited by admin on Wed Apr 02 11:13:04 GMT 2025
|
PRIMARY | |||
|
219-424-4
Created by
admin on Wed Apr 02 11:13:04 GMT 2025 , Edited by admin on Wed Apr 02 11:13:04 GMT 2025
|
PRIMARY |