| Weight | 152.193 g/mol |
|---|---|
| Formula | C9H12O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
1125-21-9 (1125-21-9)
ketoisophorone
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- Old Yellow Enzyme from Candida macedoniensis catalyzes the stereospecific reduction of the C=C bond of ketoisophorone. (Bioscience, Biotechnology, and Biochemistry, 2002)
- Synthesis of (R)- and (S)-4-hydroxyisophorone by ruthenium-catalyzed asymmetric transfer hydrogenation of ketoisophorone (Tetrahedron-asymmetry, 2000)
- Unprecedented selectivity behaviour in the hydrogenation of an , -unsaturated ketone : hydrogenation of ketoisophorone over alumina-supported Pt and Pd (Journal of Molecular Catalysis A-chemical, 1999)
- Advances in homogeneous and heterogeneous catalytic aerobic oxidation of isophorone to ketoisophorone (Journal of Molecular Catalysis A-chemical, 2002)
- Metal and solvent-free oxidation of -isophorone to ketoisophorone by molecular oxygen (Catalysis Communications, 2010)
- Light-Driven, Quantum Dot-Mediated Regeneration of FMN To Drive Reduction of Ketoisophorone by Old Yellow Enzyme (ACS Catalysis, 2012)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - ketoisophorone
-
SMILESCC1=CC(=O)CC(C1=O)(C)C
-
InChIKeyAYJXHIDNNLJQDT-UHFFFAOYSA-N
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Alternate Names
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Synthesis
4-Hydroxy-2,6,6-trimethylcyclohex-2-en-1-one
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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1125-21-9
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