Van der Pers, J. N. C. et al. published their research in Entomologia Experimentalis et Applicata in 1982 | 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.Name: (E)-Dodeca-9,11-dien-1-yl acetate

Comparison of single cell responses of antennal sensilla trichodea in the nine European small ermine moths (Yponomeuta spp.) was written by Van der Pers, J. N. C.. And the article was included in Entomologia Experimentalis et Applicata in 1982.Name: (E)-Dodeca-9,11-dien-1-yl acetate The following contents are mentioned in the article:

Single cell recordings were made from antennal sensilla trichodea of males of the 9 European small ermine moths by the tip-recording technique. Seventeen chem. were used as stimuli. Two or 3 electrophysiol. types of sensilla trichodea were found in each species. The response spectra of the receptor cells in these sensilla differed both intra- and interspecifically. Most cell types were sensitive to ≥2 substances, but some types were activated by one substance only. The results suggest that the various species use different multicomponent female sex pheromones. cis-11-Tetradecen-1-ol-acetate and trans-11-tetradecen-1-ol acetate are common components of these pheromones. Reproductive isolation in Yponomeuta may be maintained by different blends of these substances and/or the presence of addnl. compounds This study involved multiple reactions and reactants, such as (E)-Dodeca-9,11-dien-1-yl acetate (cas: 50767-78-7Name: (E)-Dodeca-9,11-dien-1-yl acetate).

(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.Name: (E)-Dodeca-9,11-dien-1-yl acetate

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