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« Previous CompoundE11-16Ac    Next Compound »E11-16OH
 
Compound - E11-16Ald
 


Bedoukain

 
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(E)-11-Hexadecenal
(E)-11-Hexadecenal

Formula: C16H30O 
CAS#: 57491-33-5 
MW: 238.41 

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





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Reference(s) for synthesis of (E)-11-Hexadecenal



Cabrera, A., Eiras, A.E., Gries, G., Gries, R., Urdaneta, N., Miras, B., Badji, C., and Jaffe, K. 2001. Sex Pheromone of tomato fruit borer, Neoleucinodes elegantalis. J. Chem. Ecol. 27:2097-2108.
 
Chou, S.-S.P., Wang. C.-J., and Hung, J.-T. 1985. Stereoselective synthesis of the sex pheromone of Heliothis armigera. Fu Jen Stud. O. 57.
 
Dunkelblum, E., Gothilf, S., and Kehat, M. 1980. Identification of the sex pheromones of the cotton bollworm Heliothis armigera in Israel. Phytoparasitica. 8:209.
 
Gothilf, S., Kehat, M., and Dunkelblum, E., and Jacobson, M. 1979. Efficacy of (Z)-11-hexadecenal and (Z)-11-tetradecenal as sex attractants for Heliothis armigera on two different dispensers. J. Econ. Entomol. 72:718.
 
Konyukhov, V.P., Kovalev, B.G., Minyailo, V.A., Stan, V.V., and Oprunenko, Yu.F. 1978. The synthesis of cis-9-tetradecenal and cis-11-hexadecenal and the determination of the effect on the cotton bollworm using the electroantennogram method. Khemoretsept. Nasek. 37.
 
Leadbetter, G. and Plimmer, J. R. 1979. An improved preparation of some insect sex attractants synthesis and separation of geometrical isomers by formation of urea complexes. J. Chem. Ecol. 5:101-108.
 
Liu, L., Lin, G., Wang, X., and Guo, G. 1985. High purity synthesis of the major components of the sex pheromone of old world bollworm (Heliothis armigera). Huaxue Xuebao. 400.
 
Liu, M., Meng, X., and Tan, Z. 1984. Synthesis of the sex pheromone of the yellow peach moth, (E)-10-hexadecenal and its (Z)-isomer. Kexue Tongbao. 29:426.
 
Ohta, K., Tatsuki, S., Uchiumi, K., Kurihara, M., and Fukami, J. 1976. Structures of sex pheromones of rice stem borer. Agric. Biol. Chem. 40:1897.
 
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.
 
Sorochinskaya, A.M., and Kovalev, B.G. 1991. J. Org. Chem. USSR (Engl. Transl.). 27:621-624.
 
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.
 
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.
 
Tumlinson, J.H., Hendricks, D.E., Mitchell, E.R., Doolittle, R.E., and Brennan, M.M. 1975. Isolation, identification, and synthesis of the sex pheromone of the tobacco budworm. J. Chem. Ecol. 1:203-214.
 

 
Citation: El-Sayed AM 2014. The Pherobase: Database of Insect Pheromones and Semiochemicals. <http://www.pherobase.com>.
2003-2014 The Pherobase - Extensive Database of Insect Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 23-February-2014