Substance

ID:714048

Names and Identifiers
IUPAC Traditional name
medon
IUPAC name
5,5-dimethylcyclohexane-1,3-dione
Synonyms
5,5-Dimethyl-1,3-cyclohexanedione双甲酮Dimedone
Registration numbers
CAS Number
MDL Number
EC Number
Beilstein Number
Merck Index
Properties
Safety Information
RTECS
GV0345000
TSCA Listed
Physical Property
Melting Point
146-150°C
Product Information
Purity
98%
Molecule Details
No Data Available
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Molecular Spectra
No Data Available
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References
• For conditions leading to exclusive 2-monomethylation, see: Synth. Commun., 3, 347 (1973). For direct nitration at the 2-position, see review on ɑ-nitroketones: Synthesis, 261 (1980).
• A comparative study has shown that CAN is superior to Mn(OAc)3 for this type of reaction: J. Chem. Soc., Perkin 1, 1487 (1996).
• Undergoes an example of an oxidative addition of 1,3-dicarbonyl compounds, mediated by CAN (Cerium(IV) ammonium nitrate, A12882), to give an alkene, e.g. with 2-methyl-2-pentene, the product is a fused dihydrofuran derivative: J. Chem. Soc., Perkin 1, 187 (1995):
• Classical reagent for the identification and isolation of aldehydes: J. Org. Chem., 11, 95 (1946).