Weight | 176.986 g/mol |
---|---|
Formula | C6H2Cl2O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
2,5-Dichloro-1,4-benzoquinone (615-93-0)
2,5-DCBQ · 2,5-dichlorobenzoquinone
Score:
#7071 in Chemistry
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- Sigma-Aldrich - 2,5-Dichloro-1,4-benzoquinone36.90 - 160.00 USD
- Fisher Scientific - Search for 2,5-Dichloro-1,4-benzoquinone
- TCI - 2,5-Dichloro-1,4-benzoquinone42.00 - 122.00 USD
- Old reagents, new results: Aromatization of Hantzsch 1,4-dihydropyridines with manganese dioxide and 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (Tetrahedron, 1995)
- 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone, a mild catalyst for the formation of carbon-nitrogen bonds (Tetrahedron, 1995)
- Selective oxidation of benzylic and allylic alcohols using Mn(OAc)3/catalytic 2,3-dichloro-5,6-dicyano-1,4-benzoquinone. (Organic Letters, 2011)
- 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone-catalyzed reactions employing MnO2 as a stoichiometric oxidant. (Organic Letters, 2010)
- Validated spectrophotometric methods for the determination of amlodipine besylate in drug formulations using 2,3-dichloro 5,6-dicyano 1,4-benzoquinone and ascorbic acid (Journal of Pharmaceutical and Biomedical Analysis, 2003)
- Selective oxidation of unsaturated alcohols catalyzed by sodium nitrite and 2,3-dichloro-5,6-dicyano-1,4-benzoquinone with molecular oxygen under mild conditions. (Journal of Organic Chemistry, 2012)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2,5-DCBQ
- 2,5-dichlorobenzoquinone
-
SMILESC1=C(C(=O)C=C(C1=O)Cl)Cl
-
InChIKeyLNXVNZRYYHFMEY-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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