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45895

Sigma-Aldrich

Farnesyl acetate

technical, mixture of isomers

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About This Item

Empirical Formula (Hill Notation):
C17H28O2
CAS Number:
Molecular Weight:
264.40
Beilstein:
1784823
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

grade

technical

refractive index

n20/D 1.477

density

0.91 g/mL at 20 °C (lit.)

SMILES string

CC(=O)OC\C=C(/C)CC\C=C(/C)CC\C=C(\C)C

InChI

1S/C17H28O2/c1-14(2)8-6-9-15(3)10-7-11-16(4)12-13-19-17(5)18/h8,10,12H,6-7,9,11,13H2,1-5H3/b15-10+,16-12+

InChI key

ZGIGZINMAOQWLX-NCZFFCEISA-N

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Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

203.0 °F - closed cup

Flash Point(C)

95 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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K Nishioka et al.
Radioisotopes, 37(3), 133-139 (1988-03-01)
Farnesylacetic acid was efficiently labelled with 14C at the 5-position and gefarnate, a potent ulcer inhibitor, was prepared from it in radioactive form for use in metabolic studies. Condensation of [carbonyl-14C]acetyl chloride (5) with t-butyl 2-ethoxymagnesiomalonate (6) followed by acid-catalyzed
Lunzhao Yi et al.
Food chemistry, 186, 192-199 (2015-05-16)
This paper introduces a detailed method to apply metabolic profiles conducting on tangerine peels (Citrus reticulata 'Dahongpao') at three maturity stages from July to December. Principal component analysis not only demonstrated the metabolic footprints of tangerine peels during ripening but
Practical synthesis of Ambrox? from farnesyl acetate involving lipase catalyzed resolution.
Tanimoto H and Oritani T.
Tetrahedron Asymmetry, 7(6), 1695-1704 (1996)
[Method of determining residues of a synthetic insecticide attractant in environmental objects].
I A Albul
Gigiena i sanitariia, (1)(1), 54-55 (1983-01-01)
Jae Soon Kang et al.
Pesticide biochemistry and physiology, 105(1), 50-56 (2013-11-19)
To understand the nematicidal mode of action of phytochemicals derived from plant essential oils against the pinewood nematode (Bursaphelenchus xylophilus), we evaluated 97 compounds (49 monoterpenes, 17 phenylpropenes, 16 sesquiterpenes, and 15 sulfides) for their inhibitory effects on B. xylophilus

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