Weight | 196.29 g/mol |
---|---|
Formula | C12H20O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 5 |
GERANYL ACETATE
33843-18-4, 16409-44-2, 68311-13-7, 105-87-3
Score:
#711 in Biochemistry
,
#2414 in Chemistry
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- Kinetics of geranyl acetate synthesis by lipase-catalysed transesterification in n-hexane (Enzyme and Microbial Technology, 1992)
- Geranyl acetate synthesis by lipase-catalyzed transesterification in supercritical carbon dioxide (Enzyme and Microbial Technology, 1993)
- Enzymatic synthesis of geranyl acetate inn-hexane withCandida antarctica lipases (Journal of the American Oil Chemists' Society, 1994)
- OsO4-Catalyzed oxidative cyclization of geranyl and neryl acetate to cis-2,5-bis(hydroxymethyl)tetrahydrofurans (Tetrahedron Letters, 1998)
- Lipase-catalyzed synthesis of geranyl acetate in n-hexane with membrane-mediated water removal (Biotechnology and Bioengineering, 2001)
- Production of geranyl acetate and other acetates by direct esterification catalyzed by mycelium of Rhizopus delemar in organic solvent (Biotechnology Letters, 1998)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(=CCCC(=CCOC(=O)C)C)C
-
InChIKeyHIGQPQRQIQDZMP-UHFFFAOYSA-N
- Pubchem - GERANYL ACETATE
- Wikipedia - geranyl acetate
Geranyl acetate is a natural organic compound that is classified as a monoterpene. It is a colorless liquid with a pleasant floral or fruity rose aroma. Its condensed liquid has a slightly yellow color.
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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