45895
金合欢醇乙酸酯
technical, mixture of isomers
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经验公式（希尔记法）:
C17H28O2
化学文摘社编号:
分子量:
264.40
EC Number:
249-689-1
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1784823
MDL number:
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
SMILES string
CC(=O)OC\C=C(/C)CC\C=C(/C)CC\C=C(\C)C
grade
technical
refractive index
n20/D 1.477
density
0.91 g/mL at 20 °C (lit.)
Quality Level
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存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
203.0 °F - closed cup
flash_point_c
95 °C - closed cup
ppe
Eyeshields, Gloves
Christos Raptis et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 15(44), 11918-11927 (2009-09-26)
Based on stereoisotopic studies and beta-secondary isotope effects, we propose that the acid-catalyzed cyclization of geranyl acetate proceeds through a concerted mechanism. Under heterogeneous conditions (zeolite Y confinement), a preorganized chairlike transition state predominates, whereas under homogeneous conditions the boat-
Yonghong Xiao et al.
Journal of chemical ecology, 35(7), 769-778 (2009-07-07)
Chemical signaling plays an important role in spider sexual communication, yet the chemistry of spider sex pheromones remains poorly understood. Unlike insects and mammals, the identification of spider pheromones has seldom been attempted, and no multicomponent pheromones have been found.
The biogenetically patterned in vitro oxidation-cyclization of farnesyl acetate.
van Tamelen EE, et al.
Journal of the American Society of Brewing Chemists, 85(20), 3295-3296 (1963)
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
T E Meigs et al.
Experimental cell research, 219(2), 461-470 (1995-08-01)
Cells treated with compactin, an inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase, the enzyme which catalyzes the rate-limiting step of the mevalonate pathway, are arrested prior to the DNA synthesis (S) phase of the cell cycle. Identification of a specific
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