Li, Xing-Long et al. published their research in Green Chemistry in 2018 | CAS: 106-79-6

Dimethyl decanedioate (cas: 106-79-6) 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. 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 106-79-6

Synthesis of medium-chain carboxylic acids or α,ω-dicarboxylic acids from cellulose-derived platform chemicals was written by Li, Xing-Long;Zhang, Kun;Jiang, Ju-Long;Zhu, Rui;Wu, Wei-Peng;Deng, Jin;Fu, Yao. And the article was included in Green Chemistry in 2018.Application of 106-79-6 This article mentions the following:

Medium-chain fatty acids and their derivatives have important applications in the energy and chem. industries. Thus, a series of medium-chain fatty acids were prepared by the selective hydrodeoxygenation of the aldol condensation products derived from cellulose using a metal triflate and Pd/C catalyst system. The selective retention of the carboxyl group is a notable feature of this catalytic system. In the experiment, the researchers used many compounds, for example, Dimethyl decanedioate (cas: 106-79-6Application of 106-79-6).

Dimethyl decanedioate (cas: 106-79-6) 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. 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 106-79-6

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