T6601
3,4,5,6-Tetrachloro-1,2-benzoquinone
97%
Synonym(s):
o-Chloranil
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About This Item
Linear Formula:
C6Cl4(=O)2
CAS Number:
Molecular Weight:
245.88
Beilstein/REAXYS Number:
1309782
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
assay
97%
mp
126-129 °C (lit.)
storage temp.
2-8°C
SMILES string
ClC1=C(Cl)C(=O)C(=O)C(Cl)=C1Cl
InChI
1S/C6Cl4O2/c7-1-2(8)4(10)6(12)5(11)3(1)9
InChI key
VRGCYEIGVVTZCC-UHFFFAOYSA-N
Gene Information
human ... ACHE(43) , BCHE(590) , CES1(1066)
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signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Hamid R Zare et al.
The journal of physical chemistry. B, 113(23), 8080-8085 (2009-05-21)
The electrochemical reduction of o-chloranil (OCA) in aqueous solution has been studied experimentally and theoretically. The effects of temperature and pH on various thermodynamic parameters were studied by means of cyclic voltammetry. The pH dependence of the redox activity of
Dalim Kumar Roy et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 61(9), 2017-2022 (2005-05-25)
Cloxacillin sodium has been shown to form charge transfer (CT) complexes of 1:1 stoichiometry with a number of electron acceptors in 50% (v/v) aqueous ethanol medium. From the trends in the CT absorption bands, the vertical ionization potential of the
P H Lin et al.
Toxicology and applied pharmacology, 145(2), 399-408 (1997-08-01)
The dosimetry of chlorinated quinones arising from metabolism of pentachlorophenol (PCP), in the livers of male Sprague-Dawley rats and B6C3F1 mice was investigated via measurements of cysteinyl protein adducts and estimates of the second-order reaction rate constants between the quinones
B Chakraborty et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 57(2), 223-229 (2001-02-24)
The equilibrium constants, enthalpies and entropies of formation of molecular electron donor-acceptor (EDA) complexes of o-chloranil with a series of aromatic hydrocarbons have been determined spectrophotometrically. Spectroscopic and thermodynamic aspects of these complexes have been analysed.
Frank Wurche et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 10(11), 2707-2721 (2004-06-15)
The effect of pressure on the oxidation of hydroarenes 3-9 with 2,3-dichloro-5,6-dicyano-1,4-quinone (DDQ; 1 a) or o-chloranil (10), leading to the corresponding arenes, has been investigated. The activation volumes were determined from the pressure dependence of the rate constants of
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