| Weight | 262.437 g/mol |
|---|---|
| Formula | C18H30O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 9 |
Farnesyl acetone (762-29-8, 1117-52-8)
farnesylacetone · farnesylacetone, (E,E)-isomer
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- Cholinesterase inhibitory activity of two farnesylacetone derivatives from the brown alga Sargassum sagamianum (Archives of Pharmacal Research, 2003)
- Comparative effect of farnesylacetone on macromolecular synthesis in gonads of crustaceans (General and Comparative Endocrinology, 1984)
- Biosynthse de la farnsylactone(E,E) par les glandes andrognes du crabe carcinus maenas (Helvetica Chimica Acta, 1978)
- New farnesylacetone derivatives from Sargassum micracanthum. (Chemistry Letters, 1979)
- Two derivatives of farnesylacetone from the brown algaCystophora moniliformis (Cellular and Molecular Life Sciences, 1978)
- Two new farnesylacetone derivatives from the brown alga Sargassum micracanthum (Phytochemistry, 1982)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - farnesylacetone
- farnesylacetone, (E,E)-isomer
-
SMILESCC(=CCCC(=CCCC(=CCCC(=O)C)C)C)C
-
InChIKeyLTUMRKDLVGQMJU-UHFFFAOYSA-N
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Synthesis
5,9,13-Pentadecatrien-2-ol, 6,10,14-trimethyl-, (5E,9E)-
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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Farnesyl acetone
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