Exploiting the Synthetic Potential of Sesquiterpene Cyclases for Generating Unnatural Terpenoids was written by Oberhauser, Clara;Harms, Vanessa;Seidel, Katja;Schroeder, Benjamin;Ekramzadeh, Kimia;Beutel, Sascha;Winkler, Sven;Lauterbach, Lukas;Dickschat, Jeroen S.;Kirschning, Andreas. And the article was included in Angewandte Chemie, International Edition in 2018.SDS of cas: 37905-02-5 The following contents are mentioned in the article:
The substrate flexibility of eight purified sesquiterpene cyclases (STCs) was evaluated using six new heteroatom-modified farnesyl pyrophosphates, and the formation of six new heteroatom-modified macrocyclic and tricyclic sesquiterpenoids is described. Gas chromatog.-olfactory (GC-O) anal. revealed that tricyclic THF exhibits an ethereal, peppery, and camphor-like olfactoric scent. This study involved multiple reactions and reactants, such as (2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate (cas: 37905-02-5SDS of cas: 37905-02-5).
(2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate (cas: 37905-02-5) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.SDS of cas: 37905-02-5
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics