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¦ « Previous CompoundE11-14OH    Next Compound »E11-16Ald ¦
 
Compound - E11-16Ac [(E)-11-Hexadecenyl acetate]
 


Bedoukain RussellIPM
 
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(E)-11-Hexadecenyl acetate
(E)-11-Hexadecenyl acetate

Formula: C18H34O2 
CAS#: 56218-72-5 
MW: 282.47 

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





Dots surface:


Reference(s) for synthesis of (E)-11-Hexadecenyl acetate [E11-16Ac]


Bestmann, H.J, Kantardjiew, I., Roesel, P., Stransky, W., and Vostrowsky, O. 1978. Pheromone. XIII. Synthese von 1-substituierten (Z)-11-alkenen. Chem. Ber. 111:248-253.
 
Chisholm, M.D., Steck, W., and Underhill, E.W. 1980. Effects of additional double bonds on some olefinic moth sex attractants. J. Chem. Ecol. 6:203-212.
 
Dzhemilev, U.M., Balezina, G.G., Volkova, L.A., Krivonogov, V.P., and Tolstikov, G.A. 1980. Insect pheromones and their analogs. III. Synthesis of the sex attractants of some Lepidoptera. Khim. Prir. Soedin. 3:97-102.
 
Gunawardena, N.E. 1992. Convenient synthesis of (E)-11-hexadecenyl acetate, the female sex pheromone of the brinjal moth Leucinodes orbonalis Guenee. J. Nat. Sci. Council. 20:71-80.
 
Nanda, B., Butalia, M.S., Patwardhan, S.A., and Gupta, A.S. 1985. Role of pheromones in integrated pest management. Behav. Physiol. Appr. Pest Manage. Pap. Natl. Semin. 73.
 
Novak, L, Toth, M., Balla, J., and Szantay, Cs. 1979. Sex pheromone of the cabbage armyworm, Mamestra brassicae: isolation, identification and stereocontrolled synthesis. Acta Chim. Acad. Sci. Hung. 102:135.
 
Sekul, A.A., Sparks, A.N., Beroza, M., and Bierl, B.A. 1975. A natural inhibitor of the corn earworm moth sex attractant. J. Econ. Entomol. 68:603-604.
 
Steck, W., Underhill, E.W., Bailey, B.K., and Chisholm, M.D. 1977. A sex attractant for male moths of the glassy cutworm Crymodes devastator Brace: a mixture of Z-11-hexadecen-1-yl acetate, Z-11-hexadecen-1-al and Z-7-dodecen-1-yl acetate. Environ. Entomol. 6:270-273.
 
Struble, D.L., and Swailes, G.E. 1975. A sex attractant for the clover cutworm, Scotogramma trifolii (Rottenburg), a mixture of Z-11-hexadecen-1-ol acetate and Z-11-hexadecen-1-ol. Environ. Entomol. 4:632-636.
 
Tamaki, Y., Kawasaki, K., Yamada, H., Koshihara, T., Osaki, N., Ando, T., Yoshida, S., and Kakinohana, H. 1977. (Z)-11-hexadecenal and (Z)-11-hexadecenyl acetates: sex-pheromone components of the diamondback moth (Lepidoptera: Plutellidae). Appl. Entomol. Zool. 12:208-210.
 
Tolstikov, G.A., Odinokov, V.N., Galeeva, R.I., Bakeeva, R.S., and Akhunova, V.R. 1979. A new stereospecific synthesis of sex pheromones of insects of the (Z)-alkenyl-1-acetate series based on selective ozonolysis of 1-methyl-1Z,5Z-cyclooctadiene. Tetrahedron Lett. 20:4851-4854.
 
Tolstikov, G.A., Odinokov, V.N., Galeeva, R.I., Bakeeva, R.S., and Akhunova, V.R. 1982. Pheromones of insects and their analogs. V. A new approach to the synthesis of the sex pheromones of insects of the order Lepidoptera which is based on the selective ozonolysis of 1-methylcycloocta-1Z,5Z-diene. Khim. Prir. Soed. 239.
 
Ujvary, I. 1984. Synthesis of the sex pheromone of the cabbage army worm (Mamestra brassicae L.). Magy. Kem. Lapja. 39:124.
 
Vostrowsky, O., Bestmann, H.J., and Priesner, E. 1973. Struktur und aktivitaet von pheromonen. Nachr. Chem. Techn. 21:501.
 
Zakharkin, L.I., and Guseva, V.V. 1984. The synthesis of (Z)-11-tetradecen-1-ol and (Z)-11-hexadecen-1-ol from 1,12-dodecadienols. Khim. Prir. Soedin. 776.
 

 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
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