Weight | 245.876 g/mol |
---|---|
Formula | C6Cl4O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
o-Chloranil (2435-53-2)
2-chloranil · tetrachloro-o-benzoquinone · 3,4,5,6-tetrachloro-1,2-benzoquinone
Score:
#2070 in Physics
,
#6443 in Chemistry
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- Photovoltaic Properties of Porphyrin Thin Films Mixed with o-Chloranil (Bulletin of the Chemical Society of Japan, 1993)
- The Structure of Quinone-Donor Adducts. I. The Action of Triphenylphosphine on p-Benzoquinone, 2,5-Dichloro-p-benzoquinone and Chloranil (Journal of the American Chemical Society, 1956)
- Synthesis and spectroscopic structural investigations of the charge-transfer complexes formed in the reaction of 2,6-diaminopyridine with -acceptors TCNE, chloranil, and DDQ (Journal of Molecular Structure, 2007)
- Spectrophotometric determination of fluoxetine and sertraline using chloranil, 2, 3 dichloro-5, 6 dicyano benzoquinone and iodine (Journal of Pharmaceutical and Biomedical Analysis, 1999)
- Synthesis of chromans via [3 + 3] cyclocoupling of phenols with allylic alcohols using a Mo/o-chloranil catalyst system. (Organic Letters, 2009)
- CH activation route to dibenzo[a,e]pentalenes: annulation of arylacetylenes promoted by PdCl2AgOTfo-chloranil (Chemical Science, 2013)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2-chloranil
- tetrachloro-o-benzoquinone
- 3,4,5,6-tetrachloro-1,2-benzoquinone
-
SMILESC1(=C(C(=O)C(=O)C(=C1Cl)Cl)Cl)Cl
-
InChIKeyVRGCYEIGVVTZCC-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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