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It was first prepared by Robert Evert and Victor Merz in 1876 by hydrolysis of 2,6-dicyanonaphthalene. [2] [3] 1,8-Naphthalenedicarboxylic acid can be isomerized to 2,6-naphthalenedicarboxylic acid via the intermediacy of the dipotassium dicarboxylates. [2] It is also produced by oxidation of 2,6-diisopropylnaphthalene. [4]
propane-1,3-dicarboxylic acid n-pyrotartaric acid: HOOC(CH 2) 3 COOH 2-oxopentanedioic acid: α-ketoglutaric acid 2-ketoglutaric acid 2-oxoglutaric acid oxoglutaric acid: HOOC(CH 2) 2 COCOOH 3-oxopentanedioic acid: acetonedicarboxylic acid 3-oxoglutaric acid β-ketoglutaric acid 3-ketoglutaric acid: HOOCCH 2 COCH 2 COOH furan-2-carboxylic acid ...
This dicarboxylic acid was shown to be a potent wound healing agent in plant that stimulates cell division near a wound site, [18] it derives from 18:2 or 18:3 fatty acid hydroperoxides after conversion into oxo- fatty acids.
Dibasic ester or DBE is an ester of a dicarboxylic acid.Depending on the application, the alcohol may be methanol or higher molecular weight monoalcohols. Mixtures of different methyl dibasic esters are commercially produced from short-chain acids such as adipic acid, glutaric acid, and succinic acid. [1]
In the example, there is a bromo-substituted -CH 2-CH 2 - subunit. 1-Bromoethane-1,2-diyl is chosen in preference to 2- bromoethane-1,2-diyl as the former has a lower locant for the bromo-substituent. The preferred CRU is therefore oxy(1-bromoethane-1,2-diyl) and the polymer is thus named poly[oxy(1-bromoethane-1,2-diyl)].
Two major manufacturing routes exist for polyethylene naphthalate (PEN), i.e. an ester or an acid process, named according to whether the starting monomer is a diester or a diacid derivative, respectively. In both cases for PEN, the glycol monomer is ethylene glycol.
Penta-2,3-dienedioic acid (one of two chemicals called glutinic acid), is an allene-containing dicarboxylic acid. It was the first allene to be synthesized, in 1887, but the structure of it was thought to be a propyne core instead of an allene. The correct structural isomeric identity was not determined until 1954. [1]
Poly(ethylene succinate) (PES) is an aliphatic synthetic polyester with a melting point from 103–106 °C. It is synthesized from dicarboxylic acids; either by ring-opening polymerization of succinic anhydride with ethylene oxide or by polycondensation of succinic acid and ethylene glycol. [1]