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Compound - Z5-10Ac


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(Z)-5-Decenyl acetate
(Z)-5-Decenyl acetate

Formula: C12H22O2 
CAS#: 67446-07-5 
MW: 198.3 

[MS]  [ NMR ]  [ Kovats ]  [Behavioural function]  [Chemdraw

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Reference(s) for synthesis of (Z)-5-Decenyl acetate

Bestmann, H.J., Vostrowsky, O., Koschatzky, K.-H., Platz, H., Brosche, T., Kantardjiew, I., Rheinwald, M., and Knauf, W. 1978. (Z)-5-decenylacetat, ein sexuallockstoff fur maennchen der saateule Agrotis segetum. Angew. Chem. 90:815.
Botar, A.A., Oprean, B.I., Csonka-Horvai, J., and Hodosan, F. 1983. Exo- and endohormones. Vl. Syntheses of the sex pheromones of some Lepidoptera. Rev. Roum. Chim. 28:741.
Buss, A.D., Greeves, N., Levin, D., Wallace, P., and Warren, S. 1984. Synthesis of single isomers (E or Z) of unsaturated alcohols by the Horner-Wittig reaction. Tetrahedron Lett. 25:357-360.
Kovalev, B.G., Dzhumakulov, T., and Abduvakhabov, A.A. 1986. Synthesis of cis-dec-5-en-1-ol acetate - one of the components of the sex pheromone of Agrotis segetum. Khim. Prir. Soedin. 122.
Odinokov, V.N., Baletsia, G.G., Ishmuratov, G.U., Vaxitov, R.S., and Tolstikov, C.A. 1985. Pheromones of insects and their analogs. XII. Synthesis, of isomers of 5-decenylacetate, pheromone of Anarsia lineatella and Agrotis segetum. Khim. Prir. Soedin. 395-398.
Odinokov, V.N., Galeeva, R.I., Sokol'skaya, O.V., Dzhemileva, G.A., and Tolstikov, G.A. 1985. A new stereospecific synthesis of 5Z-decenyl acetate, the sex pheromone of the winter moth (Agrotis segetum). Dokl. Akad. Nauk. SSSR. 280:646.
Steck, W.F., Underhill, E.W., Chisholm, M.D., and Byers, J.R. 1979. Sex attractants for Agrotis venerabilis and Euxoa albipennis based on (Z)-5-decenyl acetate and (Z)-7-dodecenyl acetate. Environ. Entomol. 8:1126-1128.
Tortajada, A., Mestres, R., and Iglesias-Arteaga, M.A. 2003. Synthesis of (Z)-5-decenol and (Z)-5-decenyl acetate, components of the sex pheromones of a variety of Lepidoptera. Synth. Comm. 33:1809-1814.
Wakamura, J. 1980. Sex attractant pheromone of the common cutworm moth Agrotis fucosa Butler: field evaluation. Appl. Entomol. Zool. 15:167.
Wenkert, E., Ferreira, V.F., Michelotti, E.L., and Tingoli, M. 1985. Synthesis of acyclic, cis olefinic pheromones by way of Nickel-catalyzed Grignard reactions. J. Org. Chem. 50:719-721.
Yu, H., Zang, B., and Han, X. 1983. Scientific notes on the synthesis of sex pheromone of Euxoa segetum (Schiffermuller) and activity test in the field. K'un Ch'ung Chih. Shih. 20:105.

Citation: El-Sayed AM 2018. The Pherobase: Database of Pheromones and Semiochemicals. <>.
2003-2018 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
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