Practical synthesis of 1,5-dimethyl substituted conjugated polyenes from geranyl acetate was written by Zhao, Yu-Jun;Loh, Teck-Peng. And the article was included in Tetrahedron in 2008.Application of 37905-02-5 The following contents are mentioned in the article:
A protocol to synthesize 1,5-di-Me substituted conjugated polyenes via dehydrogenation of geranyl acetate was established. C5 unit elongation to multi-1,5-dimethyl substituted conjugated polyenes, e.g. I, was also achieved via Horner-Wadsworth-Emmons olefination in good yields and good selectivities. This study involved multiple reactions and reactants, such as (2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate (cas: 37905-02-5Application of 37905-02-5).
(2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate (cas: 37905-02-5) 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 37905-02-5
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics