| Weight | 194.318 g/mol |
|---|---|
| Formula | C13H22O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 6 |
Geranylacetone (3796-70-1, 689-67-8)
geranylacetone, (E)-isomer
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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)
- Biotransformations of acyclic terpenoids, (+/-)-trans-nerolidol and geranylacetone, by Glomerella cingulata (Journal of Agricultural and Food Chemistry, 1996)
- A geranylacetone derivative from the brown alga Cystoseira crinita (Phytochemistry, 1980)
- Protective effects of heat shock protein70 induced by geranyl- geranylacetone in atrophic gastritis in rats (Acta Pharmacologica Sinica, 2007)
- Microbial Oxidation of Geranylacetone and Geranyloxycoumarin, Aurapten (Bulletin des Socits Chimiques Belges, 2010)
- The Algal Excretion Product, Geranylacetone: A Potent Inhibitor of Carotene Biosynthesis in Synechococcus (Zeitschrift fr Naturforschung C, 1979)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - geranylacetone, (E)-isomer
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SMILESCC(=CCCC(=CCCC(=O)C)C)C
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InChIKeyHNZUNIKWNYHEJJ-UHFFFAOYSA-N
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Similar Compounds
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Geranylacetone
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