Magro, A. Alberto Nunez et al. published their research in Chemical Science in 2010 | CAS: 106-79-6

Dimethyl decanedioate (cas: 106-79-6) 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. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Application of 106-79-6

Highly selective formation of unsaturated esters or cascade reactions to α,ω-diesters by the methoxycarbonylation of alkynes catalyzed by palladium complexes of 1,2-bis(ditertbutylphosphinomethyl)benzene was written by Magro, A. Alberto Nunez;Robb, Lynzi-Marie;Pogorzelec, Peter J.;Slawin, Alexandra M. Z.;Eastham, Graham R.;Cole-Hamilton, David J.. And the article was included in Chemical Science in 2010.Application of 106-79-6 This article mentions the following:

The methoxycarbonylation of phenylethyne catalyzed by Pd/1,2-bis-(ditertiarybutylphosphinomethyl)benzene gives the unusual linear product, Me cinnamate with high activity (initial turnover frequency, TOFo > 1700 mol product·(mol catalyst·h)-1) and regioselectivity (>90%). Terminal aliphatic alkynes give α,β-unsaturated esters after short reaction times or α,ω-diesters, including di-Me 1,6-hexanedioate (di-Me adipate), from 1-butyne after longer times. The diesters are formed by a cascade methoxycarbonylation-isomerization-methoxycarbonylation sequence. Methoxycarbonylation of internal alkynes (e.g. 4-octyne) gives the mono-carbonylated product as a result of the low propensity of the tri-substituted double bond of the product towards isomerization. Hydroxycarbonylation of phenylethyne gives predominantly E-3-phenylpropanoic acid with smaller amounts of branched and disubstituted products as well as 3-phenylpropanoic acid. Evidence is presented that the reactions occur via a hydride mechanism. 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 typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Application of 106-79-6

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