128198
Ethyl chrysanthemate
95%
Synonym(s):
2,2-Dimethyl-3-(1-isobutenyl)cyclopropane-1-carboxylic acid ethyl ester, Chrysanthemum monocarboxylic acid ethyl ester
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About This Item
Empirical Formula (Hill Notation):
C12H20O2
CAS Number:
Molecular Weight:
196.29
EC Number:
202-579-7
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
2045740
MDL number:
assay
95%
refractive index
n20/D 1.461 (lit.)
bp
112 °C/10 mmHg (lit.)
density
0.906 g/mL at 25 °C (lit.)
SMILES string
CCOC(=O)C1C(\C=C(\C)C)C1(C)C
InChI
1S/C12H20O2/c1-6-14-11(13)10-9(7-8(2)3)12(10,4)5/h7,9-10H,6H2,1-5H3
InChI key
VIMXTGUGWLAOFZ-UHFFFAOYSA-N
General description
Ethyl chrysanthemate is an allelochemical compound used as an attractant.
Application
Ethyl chrysanthemate was used in the preparation of trans-2,2-dimethylcyclopropyl nucleosides.
Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_f
183.2 °F - closed cup
flash_point_c
84 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
Regulatory Information
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J P Morin et al.
Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie, 319(7), 595-602 (1996-07-01)
Ethyl 4-methyloctanoate, which has already been described in Oryctes monoceros, has been identified, using extracts of effluvia collected from males, as being a major component of the male pheromone of O. rhinoceros. Field trials have been carried out in North
Min Chul Kook et al.
Archives of pharmacal research, 26(11), 887-891 (2003-12-10)
Novel trans-2,2-dimethylcyclopropyl nucleosides were synthesized as potential antiviral agents. The key intermediate, 3, was synthesized via five steps from ethyl chrysanthemate and condensed with purine bases using the Mitsunobu reaction to give six cyclopropyl nucleosides. These synthesized nucleosides did not
[Determination of chrysanthemic acid and its ethyl ester in the air of a work area].
N Ia Smoliar
Gigiena i sanitariia, (3)(3), 42-43 (1988-03-01)