Lavandulyl acetate

Last updated
Lavandulyl acetate
Lavandulyl acetate.svg
Names
IUPAC name
2-Isopropenyl-5-methyl-4-hexen-1-yl acetate
Other names
5-Methyl-2-(1-methylethenyl)-4-hexen-1-ol acetate
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.043.010 OOjs UI icon edit-ltr-progressive.svg
PubChem CID
UNII
  • InChI=1S/C12H20O2/c1-9(2)6-7-12(10(3)4)8-14-11(5)13/h6,12H,3,7-8H2,1-2,4-5H3
    Key: HYNGAVZPWWXQIU-UHFFFAOYSA-N
  • InChI=1/C12H20O2/c1-9(2)6-7-12(10(3)4)8-14-11(5)13/h6,12H,3,7-8H2,1-2,4-5H3
    Key: HYNGAVZPWWXQIU-UHFFFAOYAB
  • O=C(OCC(\C(=C)C)C/C=C(/C)C)C
Properties
C12H20O2
Molar mass 196.290 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Lavandulyl acetate is the acetate ester of lavandulol. [1] It is a component of lavender oil. [2]

References

  1. ↑ Veselovskii, V. V.; Dragan, V. A.; Moiseenkov, A. M. (1990-08-01). "Synthesis of E/Z-sesquilavandulols from the product of the ene reaction of lavandulyl acetate with phenylsulfinyl chloride" . Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science. 39 (8): 1734–1736. doi:10.1007/BF00961515. ISSN   1573-9171. S2CID   197304119.
  2. ↑ Dušková, Elena; Dušek, Karel; Indrák, Přemysl; Smékalová, Kateřina (2016-01-01). "Postharvest changes in essential oil content and quality of lavender flowers" . Industrial Crops and Products. 79: 225–231. doi:10.1016/j.indcrop.2015.11.007. ISSN   0926-6690.
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