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¦ « Previous CompoundE,E-farnesal    Next Compound »E,E-farnesyl acetate ¦
 
Compound - E,E-farnesol [(E,E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol]
 


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(E,E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol
(E,E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol

Formula: C15H26O 
CAS#: 106-28-5 
MW: 222.37 

[MS]  [ NMR ]  [ Kovats ]  [Behavioural function]  [Occurrence in flower





Dots surface:


Reference(s) for synthesis of (E,E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol [E,E-farnesol]


Burrell, J.W.K., Garwood, R.F., Jackman, L.M., Oskay, E., and Weedon, B.C.L. 1966. Carotenoids and related compounds. Part XIV. Stereochemistry and synthesis of geraniol, nerol, farnesol, and phytol. J. Chem. Soc. Org. C: 2144-2154.
 
Negishi, E.-I., Valente, L.F., and Kobayashi, M. 1980. Palladium-catalyzed cross-coupling reaction of homoallylic or homopropargylic organozincs with alkenyl halides as a new selective route to 1,5-dienes and 1,5-enynes. J. Am. Chem. Soc. 102:3298-3299.
 
Saplay, K.M., Damodaran, N.P., and Dev, S. 1983. Photochemical transformations-III: organic iodides (part 3): geranyl and neryl iodides and 2(E), 6(E)- and 2(Z), 6(E)-farnesyl iodides. Tetrahedron. 39:2999-3004.
 
Suga, T., and Shishibori, T. 1980. Structure and biosynthesis of cleomeprenols from the leaves of Cleome spinosa. J. Chem. Soc.Perkin Trans. 1:2098-2104.
 

 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
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