In 1964,Ricerca Scientifica, Parte 2: Rendiconti, Sezione A: Abiologica included an article by Chierici, Luigi; Scapini, Giancarlo. Safety of Dimethyl 1H-pyrrole-2,3-dicarboxylate. The article was titled 《Chromatographic study of pyrrole acids. Gas chromatography of the C-pyrrolecarboxylic acids》. The information in the text is summarized as follows:
Mixtures of C-pyrrolecarboxylic acids are separated as Me esters on a 100-cm. column packed with 3% ethylene-glycol-succinate on Chromosorb W. The instrument is operated with a 300° injection port temperature, a flame ionization detector, a 15 ml./min. N flow, and the column is temperature-programmed from 150 to 210° at 25°/min. The temperature program starts after separation of the 2-pyrrolecarboxylic acid.Dimethyl 1H-pyrrole-2,3-dicarboxylate(cas: 2818-08-8Safety of Dimethyl 1H-pyrrole-2,3-dicarboxylate) was used in this study.
Dimethyl 1H-pyrrole-2,3-dicarboxylate(cas: 2818-08-8) belongs to pyrroles. Pyrroles are components of more complex macrocycles, including the porphyrinogens and products derived therefrom, including porphyrins of heme, the chlorins, bacteriochlorins, and chlorophylls. Porphobilinogen, a trisubstituted pyrrole, is the biosynthetic precursor to many natural products such as heme.Safety of Dimethyl 1H-pyrrole-2,3-dicarboxylate
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics