| Weight | 154.253 g/mol |
|---|---|
| Formula | C10H18O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 5 |
Myrcenol (543-39-5)
2-methyl-6-methyleneoct-7-en-2-ol · 3-methylene-7-methyl-1-octen-7-ol · 7-hydroxy-7-methyl-3-methylene-1-octene
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- E-Myrcenol in Ips duplicatus: an aggregation pheromone component new for bark beetles. (Cellular and Molecular Life Sciences, 1990)
- Demonstration of de Novo pheromone biosynthesis in Ips duplicatus (Coleoptera: Scolytidae): inhibition of Ipsdienol and E-Myrcenol production by compactin (Insect Biochemistry and Molecular Biology, 1993)
- Sex-specific production of ipsdienol and myrcenol byDendroctonus ponderosae (Coleoptera: Scolytidae) exposed to myrcene vapors. (Journal of Chemical Ecology, 1986)
- E-Myrcenol: a new pheromone for the pine engraver, Ips pini (Say) (Coleoptera: Scolytidae). (Canadian Entomologist, 1990)
- On a sulfurated grignard reagent equivalent to that of 2-chloromethyl-1,3-butadiene. New syntheses of ipsenol (2-methyl-6-methylene-7-octen-4-OL) and of (E)--farnesene ((E)-7,11-dimethyl-3-methylene-1,6,10-dodecatriene) (Journal of Organometallic Chemistry, 1979)
- A practical synthesis of myrcenol by palladium complex-catalyzed elimination reaction. (Chemistry Letters, 1986)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2-methyl-6-methyleneoct-7-en-2-ol
- 3-methylene-7-methyl-1-octen-7-ol
- 7-hydroxy-7-methyl-3-methylene-1-octene
- 7-methyl-3-methylene-1-octen-7-ol
-
SMILESCC(C)(CCCC(=C)C=C)O
-
InChIKeyDUNCVNHORHNONW-UHFFFAOYSA-N
- Pubchem - Myrcenol
- Wikipedia - myrcenol
Myrcenol is an organic compound, specifically a terpenoid. It is most notable as one of the fragrant components of lavender oil. It is also found in the hop plant (Humulus lupulus).
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