Dondoy, J.; Alloing-Bernard, A.; Renson-Deneubourg, C. published an article in 1971, the title of the article was Functional analysis and gas-chromatographic separation of perfluorinated mono- and diesters of diols.Application In Synthesis of 2,2-Dimethylpropane-1,3-diyl bis(2-methylacrylate) And the article contains the following content:
Functional analysis. methods for fluorinated esters are discussed. Perfluorocarboxylic acid esters, such as Et perfluorooctanoate, are titrated in neutralized EtOH with 0.5N alc. KOH. The error for the above compound was ±1.8%. The classical saponification method must be used for esters F3C(CF2)nCH2CO2R (R = alkyl). When the above method is used for ethylene glycol acrylate perfluorooctanoate it specifically determines the perfluorinated acid. Hydroxyl numbers are determined by HClO4-catalyzed acetylation, and residual acidity by NH4OH titration For chromatog. of the esters a suitable stationary phase is Plastinol on a Gas Pack F support. The experimental process involved the reaction of 2,2-Dimethylpropane-1,3-diyl bis(2-methylacrylate)(cas: 1985-51-9).Application In Synthesis of 2,2-Dimethylpropane-1,3-diyl bis(2-methylacrylate)
The Article related to perfluorinated ester functional analysis, acid number perfluorocarboxylic ester, hydroxyl number perfluorocarboxylic ester, functional groups and other aspects.Application In Synthesis of 2,2-Dimethylpropane-1,3-diyl bis(2-methylacrylate)
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics