| Weight | 227.006 g/mol |
|---|---|
| Formula | C8Cl2N2O2 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
84-58-2 (84-58-2)
dichlorodicyanobenzoquinone · 2,3-DDQ · 2,3-dichloro-5,6-dicyano-1,4-benzoquinone
Score:
#6054 in Chemistry
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- Kinetic acetalization for 1,2- and 1,3-diol protection by the reaction of p-methoxyphenylmethyl methyl ether with DDQ (Tetrahedron Letters, 1983)
- Characterization of the 1:1 charge-transfer reaction between decamethylferrocene and 2,3-dichloro-5,6-dicyanoquinone (DDQ): structure of the DDQH- anion (Journal of the American Chemical Society, 1982)
- 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ)/tert-Butyl Nitrite/Oxygen: A Versatile Catalytic Oxidation System (Advanced Synthesis & Catalysis, 2011)
- 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) in aqueous acetic acid, a convenient new reagent for the synthesis of aryl ketones and aldehydes via benzylic oxidation (Journal of Organic Chemistry, 1988)
- 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) oxidation of silyl enol ethers to enones via DDQ-substrate adducts (Journal of Organic Chemistry, 1989)
- A novel and highly selective conversion of alcohols, thiols, and silyl ethers to azides using the triphenylphosphine/2,3-dichloro-5,6-dicyanobenzoquinone(DDQ)/n-Bu4NN3 system (Tetrahedron Letters, 2004)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - dichlorodicyanobenzoquinone
- 2,3-DDQ
- 2,3-dichloro-5,6-dicyano-1,4-benzoquinone
- 2,3-dichloro-5,6-dicyanobenzoquinone
-
SMILESC(#N)C1=C(C(=O)C(=C(C1=O)Cl)Cl)C#N
-
InChIKeyHZNVUJQVZSTENZ-UHFFFAOYSA-N
- Pubchem - 84-58-2
- Wikipedia - 2,3-dichloro-5,6-dicyanobenzoquinone
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (or DDQ) is the chemical reagent with formula C6Cl2(CN)2O2. This oxidant is useful for the dehydrogenation of alcohols, phenols, and steroid ketones in organic chemistry. DDQ decomposes in water, but is stable in aqueous mineral acid.
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