A facile synthesis of the sex pheromone of the red bollworm moth from 10-undecen-1-ol was written by Babler, James H.;Martin, Michael J.. And the article was included in Journal of Organic Chemistry in 1977.Related Products of 50767-78-7 The following contents are mentioned in the article:
(E)-9,11-dodecadien-1-ol, whose acetate is the major component of the sex pheromone of the red bollworm moth, was prepared in six steps from 10-undecen-1-ol (I). The key step in the synthesis involved treatment of I acetate with N-bromosuccinimide to afford BrCH2CH:CH(CH2)8OAc. This study involved multiple reactions and reactants, such as (E)-Dodeca-9,11-dien-1-yl acetate (cas: 50767-78-7Related Products of 50767-78-7).
(E)-Dodeca-9,11-dien-1-yl acetate (cas: 50767-78-7) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Related Products of 50767-78-7
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics