diester

The resulting material is reacted with ethanol to form a diester.

The yellow liquid is a diester of phosphoric acid and 2-ethylhexanol.

Oil (mineral or diester based) is used as the preferred cooling and flushing media.

It is the diester of phthalic acid and the branched-chain 2-ethylhexanol.

A second S2 substitution by the benzoate anion gives the desired diester (6).

This enzyme belongs to the family of hydrolases, specifically those acting on phosphoric diester bonds.

Indeed, the dimer readily forms a six-membered cyclic diester known as lactide.

Dimethyl malonate is a diester derivative of malonic acid.

The mixture contains predominately the diester, glyceryl dibehenate.

Doxacurium is a symmetrical molecule because it is a diester of succinic acid.

It is the diester formed from the disaccharide gentiobiose and the dicarboxylic acid crocetin.

DOA is a diester of adipic acid and two equivalents of n-octanol.

This molecule, termed Autoinducer-2 (or AI-2), is a furanosyl borate diester.

Busulfan is an example of a dialkylating agent: it is the methanesulfonate diester of 1,4-butanediol.

In general, a lactide is the cyclic diester, i.e., the di-lactone of two molecules of any 2-hydroxycarboxylic acid.

When water is served as a nucleophile, the product is an H-phosphonate diester as shown in Scheme above.

The benzoyl moiety required for the formation of the cocaine diester is synthesized from phenylalanine via cinnamic acid.

Autoinducer-2 (AI-2), a furanosyl borate diester, is a member of a family of signaling molecules used in quorum sensing.

Enantioselective hydrolysis of a conjugted diester followed by ozonolysis affords the skeleton of ribose.

The diester derived from phenol, phenyl oxalate ester, is Cyalume, the active ingredient in glow sticks.

Diisopropyl tartrate (DIPT) is a diester of tartaric acid.

The Halbritters light up their bubble formula by adding a chemiluminescent agent called oxalate diester to conventional bubble blowing liquids.

A phosphoramidite (RO)PNR is a monoamide of a phosphite diester.

For instance, mevalonolactone may be synthesized rapidly from a symmetric diester via desymmetrizing hydrolysis, chemoselective reduction, and lactonization.