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« Previous CompoundZ2E13-18Ac    Next Compound »Z2Z13-18Ac
Compound - Z2E6-7me-3-propyl-10OH


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Formula: C14H26O 
CAS#: 38789-38-7 
MW: 210.36 

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

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Reference(s) for synthesis of (Z,E)-7-Methyl-3-propyl-2,6-decadien-1-ol

Bowlus, S.B., and Katzenellenbogen, J.A. 1973. A highly stereoselective synthesis of (2Z,6E)-7-methyl-3-propyl-2,6-decadien-1-ol. A proposed revision in the stereochemistry of a tetrahomoterpene isolated from the codling moth. Tetrahedron Lett. 14:1277-1280.
Bowlus, S.B., and Katzenellenbogen, J.A. 1973. Synthesis of the natural isomer of a tetrahomoterpene alcohol obtained from the codling moth. J. Org. Chem. 38:2733-2734.
Cooke, M.P., Jr. 1973. A stereoselective synthesis of a proposed codling moth sex pheromone. Tetrahedron Lett. 14:1281-1284.
Cooke, M.P., Jr. 1973. Synthetic proof of the structure of a proposed codling moth sex pheromone. Tetrahedron Lett. 14:1983-1986.
Kovalev, G.G., Khusid, A.Kh., Konyukhov, V.P., Nedopekina, S.F., and Neimark, Ya.L. 1975. Synthetic investigations in the field of sex attractants of insects. II. Synthesis of a mixture of the geometric isomers of 7-methyl-3-propyldeca-2,6-dien-1-ol, one of the components of the sex pheromone of the codling moth. Zhur. Org. Khim. 11:1183.
McDonough, L.M., George, D.A., Butt, B.A., Ruth, J.M., and Hill, K.R. 1972. Sex pheromone of the codling moth: structure and synthesis. Science. 177:177-178.
Morizur, J.-P., Muzard, G., Basselier, J.-J., and Kossanyi, J. 1975. Chimie des insects. II. Synthese du methyl-7-n-propyl-3-decadien-2(Z),6(Z)-ol-1 isole chez Laspeyresia (Carpocapsa) pomonella. Bull. Soc. Chim. Fr. 43:257.
Obayashi, M., Utimoto, K., and Nozaki, H. 1977. Magnesium iodide induced rearrangment of alpha,-epoxysilanes to -ketosilanes as applied to the stereoselective synthesis of tetrahomoterpenoid of codling moth. Tetrahedron Lett. 18:1807-1809.
Ouannes, C., and Langlois, Y. 1975. Nouvelle synthese stereoselective d'un tetrahomoterpene extrait de Laspeyresia pomonella L. et de ses trois isomeres Geometriques. Tetrahedron Lett. 16:3461-3464.
Rossi, R. 1977. Insect pheromones. I. Synthesis of achiral components of insect pheromones. Synthesis. 12:817-836.

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