| Weight | 126.199 g/mol |
|---|---|
| Formula | C8H14O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
3,3-Dimethylcyclohexanone (2979-19-3)
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- Enantioselective formation of cis-3,5-dimethylcyclohexanone lithium enolate and stereoselective aldol reaction with benzaldehyde (Journal of Organic Chemistry, 1992)
- Annelation of 2,3-dimethylcyclohexanone. Synthetic proof for the stereochemistry of the sesquiterpene aristolone (Canadian Journal of Chemistry, 1969)
- Lanthanide-induced shifts in proton nuclear magnetic resonance spectra. VI. 3-(.alpha.-Naphthyl)-5,5-dimethylcyclohexanone and derived alcohols. Synthesis and stereochemical studies by means of lanthanide-induced proton nuclear magnetic resonance shifts (Journal of the American Chemical Society, 1973)
- Enzymatic in vitro reduction of ketones: 15. The influence of reaction conditions on the stereochemical course of HLAD-catalyzed reductions: 3-Cyano-4,4-dimethylcyclohexanone as a sensitive probe (Bioorganic Chemistry, 1988)
- Infrared spectra, optical constants and semiconductor behavior of 5-(2-phenylhydrazono)-3,3-dimethylcyclohexanone thin films (Journal of Molecular Structure, 2013)
- The stereochemistry of the Michael addition reaction. The synthesis of trans-3,5 - dimethylcyclohexanone (Tetrahedron Letters, 1966)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1(CCCC(=O)C1)C
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InChIKeyZVJQBBYAVPAFLX-UHFFFAOYSA-N
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