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Key Documents

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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:
2435-53-2
Peso molecular:
245.88
Beilstein/REAXYS Number:
1309782
EC Number:
219-424-4
MDL number:
MFCD00001646
UNSPSC Code:
12352100
PubChem Substance ID:
24900391
NACRES:
NA.22

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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pictograms

Exclamation markEnvironment
GHS07,GHS09

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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Certificados de análisis (COA)

Lot/Batch Number
MKCQ4456
MKCQ2946
MKCN5217
MKCJ9949
MKCG9281

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Sigma-Aldrich

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2,5-Dichloro-1,4-benzoquinone

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
Tandrima Chaudhuri et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 204, 403-408 (2018-07-04)
This is the first report of UV-Vis spectral investigations of electron donor-acceptor complexes of bio active 3-Nitroso-2-phenylbenzo[d]imidazo[2,1-b]thiazole (BIT1) with chloranils, nitrobenzenes and fullerenes in DMSO medium. Well defined charge transfer (CT) absorption bands in the visible region have been sited.
K V P Pavan Kumar et al.
Carbohydrate research, 342(9), 1182-1188 (2007-03-24)
Treatment of the phosphoramidite [myo-C(6)H(6)-2-[OC(O)Ph]-1,3,5-(O(3)CH)-4,6-(O(2)P-NH-i-Pr)] with o-chloranil affords the first example of inositol-based pentacoordinate phosphorane [myo-C(6)H(6)-2-[OC(O)Ph]-1,3,5-(O(3)CH)-4,6-(O(2)P-NH-i-Pr)(1,2-O(2)C(6)Cl(4))] (9) (X-ray structure) with a trigonal bipyramidal geometry at phosphorus. The six-membered 1,3,2-dioxaphosphorinane ring with the inositol residue has an unusual boat conformation in
F Kader et al.
Journal of agricultural and food chemistry, 47(11), 4625-4630 (1999-12-20)
Caffeic acid o-quinone (CQ) was prepared by oxidation of caffeic acid with o-chloranil in organic media. The reaction between the purified CQ and cyanidin 3-glucoside (Cy 3-glc, o-diphenolic anthocyanin) was monitored by HPLC, and quantitative analyses were performed to establish
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
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