Nesbitt, Brenda F. et al. published their research in Journal of Insect Physiology in 1975 | CAS: 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. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Application of 50767-78-7

Isolation and identification of the female sex pheromones of the red bollworm moth, Diparopsis castanea was written by Nesbitt, Brenda F.;Cole, Beevor R. A.;Lester, R.;Poppi, R. G.. And the article was included in Journal of Insect Physiology in 1975.Application of 50767-78-7 The following contents are mentioned in the article:

The major female sex pheromone of D. castanea was 9,11-dodecadien-1-yl acetate (80:20 trans:cis). Minor components were trans-9-dodecen-1-yl acetate, 11-dodecen-1-yl acetate, and dodecan-1-yl acetate. This study involved multiple reactions and reactants, such as (E)-Dodeca-9,11-dien-1-yl acetate (cas: 50767-78-7Application 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. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Application of 50767-78-7

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics