THC Science

Lavandulyl acetate
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
CAS Number	25905-14-0 ;
3D model (JSmol)	Interactive image;
ChemSpider	28088;
ECHA InfoCard	100.043.010
PubChem CID	30247;
UNII	OU6ZF37MOM ;
CompTox Dashboard (EPA)	DTXSID6051932 ;
	InChI 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;
	SMILES O=C(OCC(\C(=C)C)C/C=C(/C)C)C;
Properties
Chemical formula	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). Infobox references

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

References[edit]

^ 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.
^ 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.