Pheromones. XXXIV. Synthesis of conjugated-unsaturated Lepidoptera pheromones and analogs was written by Bestmann, Hans Juergen;Suess, Joachim;Vostrowsky, Otto. And the article was included in Liebigs Annalen der Chemie in 1981.Reference of 50767-78-7 The following contents are mentioned in the article:
The title compounds, i.e. alkadienyl acetates, alkadienols, and alkadienals were prepared on the fragment assembly principle. Thus, e.g. R(CH2)nCH:CHCHO (R = OAc, n = 8, 10; R = CO2Me, n = 8) were treated with CH2:PPh3 to give R(CH2)nCH:CHCH:CH2 which were hydrolyzed or reduced to HO(CH2)nCH:CHCH:CH2 (n = 8-10). This study involved multiple reactions and reactants, such as (E)-Dodeca-9,11-dien-1-yl acetate (cas: 50767-78-7Reference 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. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Reference of 50767-78-7
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics