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Compound - 3me-6-isopropenyl-Z3,9-10Ac [(Z)-3-Methyl-6-isopropenyl-3,9-decadienyl acetate]

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(Z)-3-Methyl-6-isopropenyl-3,9-decadienyl acetate
(Z)-3-Methyl-6-isopropenyl-3,9-decadienyl acetate

Formula: C16H26O2 
CAS#: 66348-55-8 
MW: 250.38 

[MS]  [ NMR ]  [Behavioural function

Dots surface:

Reference(s) for synthesis of (Z)-3-Methyl-6-isopropenyl-3,9-decadienyl acetate [3me-6-isopropenyl-Z3,9-10Ac]

Celebuski, J., and Rosenblum, M. 1985. Carbon-carbon bond formation employing organoiron reagents. Syntheses of lavandulol and red scale pheromone. Tetrahedron. 41:5741-5746.
Hutchinson, J.H., and Money, T. 1985. A formal enantiospecific synthesis of California red scale pheromone. Can. J. Chem. 63:3182.
McCullough, D.W., Bhupathy, M., Piccolino, E., and Cohen, T. 1991. Highly efficient terpenoid pheromone syntheses via regio- and stereocontrolled processing of allyllithiums generated by reductive lithiation of allyl phenyl thioethers. Tetrahedron. 47:9727-9736.
Oppolzer, W., and Stevenson, T. 1986. Asymmetric additions of 1-alkenyl Copper reagents to chiral enoates: enantioselective synthesis of California red scale pheromone. Tetrahedron Lett. 27:1139-1140.
Roelofs, W.L., Gieselmann, M.J., Carde, A.M., Tashiro, H., Moreno, D.S., Henrick, C.A., and Anderson, R.J. 1977. Sex pheromone of the Califomia red scale, Aonidiella aurantii. Nature. 267:698.
Whittaker, M., McArthur, C.R., and Leznoff, C.C. 1985. Asymmetric synthesis towards (3Z,6R)-3-methyl-6-isopropenyl-3,9-decadien-1-yl acetate, a component of the California red scale pheromone. Can. J. Chem. 63:2844.

Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <>.
Ⓒ 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 13-February-2024