13213-81-5

Basic information

• Product Name: ethyl 1,2,5-triphenyl-1H-pyrrole-3-carboxylate
• Synonyms: ethyl 1,2,5-triphenyl-1H-pyrrole-3-carboxylate
• CAS NO: 13213-81-5
• Molecular Weight: 367.447
• Mol File: 13213-81-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: ethyl 1,2,5-triphenyl-1H-pyrrole-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 1,2,5-triphenyl-1H-pyrrole-3-carboxylate(13213-81-5)
• EPA Substance Registry System: ethyl 1,2,5-triphenyl-1H-pyrrole-3-carboxylate(13213-81-5)

Safety Data

• Hazardous Substances Data: 13213-81-5(Hazardous Substances Data)

Upstream product

• 29113-48-2 ethyl 2-benzoyl-4-oxo-4-phenylbutanoate 
• 62-53-3 aniline 
• 4687-38-1 diethyl-2,3-dibenzoylsuccinate 
• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 3556-76-1 ethyl (2Z)-3-phenyl-3-(phenylamino)prop-2-enoate 
• 70-11-1 α-bromoacetophenone 

Downstream Products

• 130850-64-5 4-Bromo-1,2,5-triphenyl-1H-pyrrole-3-carboxylic acid 
• 130850-69-0 3,4-Dibromo-1,2,5-triphenyl-1H-pyrrole 
• 83798-53-2 4-Chloro-1,2,5-triphenyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 83798-44-1 4-Bromo-1,2,5-triphenyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 130850-56-5 1,2,5-triphenyl-pyrrole-3-carboxylic acid 

Relevant articles and documents

PEROVSKITES FOR PHOTOCATALYTIC ORGANIC SYNTHESIS

Nature is capable of storing solar energy in chemical bonds via photosynthesis through a series of C—C, C—O and C—N bond-forming reactions starting from CO2 and light. Direct capture of solar energy for organic synthesis is a promising approach

An efficient procedure for the synthesis of polysubstituted pyrroles in an ionic liquid

The ionic liquid 1-butyl-3-methyl-imidazolium hydrogen sulfate, [bmim]HSO4, was used as a catalyst and reaction medium for the pyrrole synthesis, and a wide range of aliphatic, aromatic, heteroaromatic and carboxylic 1,4-diketones easily underwent condensations with aniline and ethylenediamine to form polysubstituted pyrroles. Sequential decarboxylation/Paal-Knorr pyrrole condensation was observed, which provides a new and facile approach to monoester pyrroles from 1,4-diketo-2,3-dicarboxylic acid esters.