Stereospecific synthesis of (E)-9,11-dodecadien-1-yl acetate, a sex pheromone of red bollworm (Diparopsis catenea) was written by Singh, Vasundhara;Vig, Rakesh;Trehan, I. R.;Kad, G. L.. And the article was included in Indian Journal of Chemistry in 1992.Product Details of 50767-78-7 The following contents are mentioned in the article:
Ireland-Claisen rearrangement of 3-acetoxy-11-(tetrahydropyranyloxy)undec-1-ene gives 13-(tetrahydropyranyloxy)-4(E)-tridecen-1-oic acid (I) stereospecifically. Oxidative decarboxylation of I followed by acetylation furnishes (E)-9,11-dodecadien-1-yl acetate in good yield. This study involved multiple reactions and reactants, such as (E)-Dodeca-9,11-dien-1-yl acetate (cas: 50767-78-7Product Details of 50767-78-7).
(E)-Dodeca-9,11-dien-1-yl acetate (cas: 50767-78-7) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. 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.Product Details of 50767-78-7
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics