Budzianowski, Jaromir’s team published research in Phytochemistry in 1990 | CAS: 2818-08-8

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.Application of 2818-08-8

Application of 2818-08-8On September 14, 1990 ,《Caffeoylmalic and two pyrrole acids from Parietaria officinalis》 was published in Phytochemistry. The article was written by Budzianowski, Jaromir. The article contains the following contents:

A methanolic extract from leaves and flowers of P. officinalis afforded 3 acids, namely caffeoylmalic, 1H-pyrrole-2,3-dicarboxylic, and 1-[(caffeoyloxy)(carboxy)methoxy]-1H-pyrrole-2,3,5-tricarboxylic acids. In the experimental materials used by the author, we found Dimethyl 1H-pyrrole-2,3-dicarboxylate(cas: 2818-08-8Application of 2818-08-8)

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.Application of 2818-08-8

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