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Names | |
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Preferred IUPAC name
2-Methyl-6-methylideneoct-7-en-2-ol | |
Identifiers | |
3D model (
JSmol)
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|
ChemSpider | |
ECHA InfoCard | 100.008.040 |
PubChem
CID
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|
UNII | |
CompTox Dashboard (
EPA)
|
|
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Properties | |
C10H18O | |
Molar mass | 154.24 g/mol |
Density | 0.85 g/cm3 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
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). E-Myrcenol acts also as a pheromone for bark beetles. [1]
Myrcenol is obtained synthetically from myrcene via hydroamination of the 1,3-diene followed by hydrolysis and Pd-catalysed removal of the amine. As a 1,3-diene, myrcenol undergoes Diels-Alder reactions with several dienophiles such as acrolein to give cyclohexene derivatives that are also useful fragrances. [2]
![]() | |
Names | |
---|---|
Preferred IUPAC name
2-Methyl-6-methylideneoct-7-en-2-ol | |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.008.040 |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C10H18O | |
Molar mass | 154.24 g/mol |
Density | 0.85 g/cm3 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
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). E-Myrcenol acts also as a pheromone for bark beetles. [1]
Myrcenol is obtained synthetically from myrcene via hydroamination of the 1,3-diene followed by hydrolysis and Pd-catalysed removal of the amine. As a 1,3-diene, myrcenol undergoes Diels-Alder reactions with several dienophiles such as acrolein to give cyclohexene derivatives that are also useful fragrances. [2]