| Weight | 192.302 g/mol |
|---|---|
| Formula | C13H20O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 5 |
Pseudoionone
13927-47-4, 3548-78-5, 141-10-6, 68815-62-3
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- The tomato carotenoid cleavage dioxygenase 1 genes contribute to the formation of the flavor volatiles -ionone, pseudoionone, and geranylacetone (Plant Journal, 2004)
- Cyclization of Pseudoionone by Acidic Reagents. (Industrial & Engineering Chemistry, 1946)
- Total Synthesis of Pseudoionone and an Isomeric Ketone (Journal of Organic Chemistry, 1958)
- Synthesis of Pseudoionone Homologs and Related Compounds (Journal of Organic Chemistry, 1957)
- Synthesis of 4-(2-Methyl-5-isopropenyl-1-cyclopenten-1-yl)butan-2-one. A By-Product in the Synthesis of Pseudoionone (Journal of Organic Chemistry, 1964)
- Efficient synthesis of pseudoionone by oxidative decarboxylation of allyl -ketoesters (Tetrahedron Letters, 1991)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H315: Causes skin irritation
Warning Skin corrosion/irritation - Category 2 - H361: Suspected of damaging fertility or the unborn child
Warning Reproductive toxicity - Category 2 - H411: Toxic to aquatic life with long lasting effects
Hazardous to the aquatic environment, long-term hazard - Category 2 -
SMILESCC(=CCCC(=CC=CC(=O)C)C)C
-
InChIKeyJXJIQCXXJGRKRJ-UHFFFAOYSA-N
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Synthesis
Acetonitrile
+
Reactant
(Grignard carbonyl)
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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Pseudoionone
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