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Compound - 3me9me-6-isopropenyl-E5,8-10Ac [(E)-3,9-Dimethyl-6-isopropyl-5,8-decadienyl acetate]

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(E)-3,9-Dimethyl-6-isopropyl-5,8-decadienyl acetate Formula:  C17H30O2  CAS#:  72603-87-3  MW:  266.42  [MS]  [ NMR ]  [Behavioural function]

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Reference(s) for synthesis of (E)-3,9-Dimethyl-6-isopropyl-5,8-decadienyl acetate [3me9me-6-isopropenyl-E5,8-10Ac] Anderson, R.J., and Henrick, C. A. 1979. Synthesis of (E)-3,9-dimethyl-6-isopropyl-5,8-decadien-1-yl acetate, the sex pheromone of the yellow scale. J. Chem. Ecol. 5:773-779.   Harusawa, S., Takemura, S., Osaki, H., Yoneda, R., and Kurihara, T. 1993. [3,3]-Sigmatropic ring expansion of cyclic thionocarbonates. 9. total synthesis of (±)-yellow scale pheromone via 10-membered thiolcarbonate. Tetrahedron. 49:7657-7666.   Masuda, S., Kuwahara, S., Suguro, T., and Mori, K. 1981. Stereoselective synthesis of (S,E)-6-isopropyl-3,9-dimethyl-5,8-decadienyl acetate the (S)-enantiomer of the yellow scale pheromone. Agric. Biol. Chem. 45:2515.   Millar, J.G. 1989. Application of silylcupration of alkynes to stereo- and regiospecific formation of trisubstituted alkenes. A short synthesis of yellow scale pheromone. Tetrahedron Lett. 30:4913-4914.   Mori, K., and Kuwahara, S. 1982. Synthesis of optically active forms of (E)-6-isopropyl-3,9-dimethyil-5,8-decadienyl acetate, the pheromone of the yellow scale. Tetrahedron. 38:521-525.   Suguro, T., Roelofs, W.L., and Mori, K. 1982. Stereoselective synthesis of (±)-(E)-6-isopropyl-3,9-dimethyl-5,8-decadienyl acetate, the racemate of the yellow scale pheromone, and its (Z)-isomer. Agric. Biol. Chem. 45:2509.