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Compound - Z11-18Ac
 


Bedoukain

 
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(Z)-11-Octadecenyl acetate
(Z)-11-Octadecenyl acetate

Formula: C20H38O2 
CAS#: 1775-43-5 
MW: 310.52 

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





Dots surface:


Reference(s) for synthesis of (Z)-11-Octadecenyl acetate



Azzena, F., Crotti, P., Favero, L., and Pineschi, M. 1995. Regiochemical control of the ring opening of 1,2-epoxides by means of chelating processes. 11. Ring opening reactions of aliphatic mono- and difunctionalized cis and trans 2,3- and 3,4-epoxy esters. Tetrahedron. 51:13409-13422.
 
Drießen-Hölscher, B., and Heinen, J. 1998. Selective two-phase-hydrogenation of sorbic acid with novel water soluble ruthenium complexes. J. Organomet. Chem. 570:141-146.
 
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.
 
Meinwald, J., and Meinwald, Y.C. 1966. Structure and synthesis of the major components in the hairpencil secretion of a male butterfly Lycorea ceres ceres (Cramer). J. Am. Chem. Soc. 88:1305-1310.
 
Steines, S., Englert, U., and Driessen-Hölscher, B. 2000. Stereoselective catalytic hydrogenation of sorbic acid and sorbic alcohol with new Cp*Ru complexes. Chem. Comm. 3:217-218.
 

 
Citation: El-Sayed AM 2014. The Pherobase: Database of Insect Pheromones and Semiochemicals. <http://www.pherobase.com>.
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