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Merck

T6601

Sigma-Aldrich

3,4,5,6-Tetrachloro-1,2-benzoquinone

97%

Sinónimos:

o-Chloranil

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About This Item

Fórmula lineal:
C6Cl4(=O)2
Número de CAS:
Peso molecular:
245.88
Beilstein/REAXYS Number:
1309782
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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

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pictograms

Exclamation markEnvironment

signalword

Warning

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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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
Mirosława Kot et al.
Journal of enzyme inhibition and medicinal chemistry, 21(5), 537-542 (2006-12-30)
Tetrachloro-o-benzoquinone (TCoBQ) and tetrachloro-p-benzoquinone (TCpBQ) were studied as inhibitors of jack bean urease in 20 mM phosphate buffer, pH 7.0, 1 mM EDTA, 25 degrees C. The mechanisms of inhibition were evaluated by analysis of the progress curves obtained with
Asim Kumar Ray et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 58(7), 1375-1378 (2002-06-27)
o-Chloranil has been shown to form 1:1 molecular complexes with pyridine and 2-, 3- and 4-picolines in CCl4 medium. Isosbestic points have been found but charge-transfer bands could not be detected. The formation constants of the complexes exhibit a very
B E Bengtsson et al.
Ecotoxicology and environmental safety, 15(1), 62-71 (1988-02-01)
The effects of tetrachloro-1,2-benzoquinone (TCQ), a component in bleached kraft mill effluents (BKME), on vertebral and physiological parameters were investigated in juvenile fourhorn sculpin, Myoxocephalus quadricornis L. After about 4.5 months of exposure to 0.1 and 0.5 mg TCQ/liter in
S Bhattacharya et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 57(12), 2409-2416 (2002-01-05)
Electron donor-acceptor (EDA) complex formation between o-chloranil and a series of anilines has been studied in CCl4 medium. In all the cases, EDA complexes are formed instantaneously on mixing the donor and acceptor solutions. N,N-dimethylaniline and N,N-dimethyl-p-toluidine form stable EDA

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