128807-50-1

Basic information

• Product Name: methyl 3-(4-chlorophenyl)-2,5-dioxo-4-phenyl-2,5-dihydro-1H-pyrrol-1-ylcarbamate
• Synonyms: methyl 3-(4-chlorophenyl)-2,5-dioxo-4-phenyl-2,5-dihydro-1H-pyrrol-1-ylcarbamate
• CAS NO: 128807-50-1
• Molecular Formula: C₁₈H₁₃ClN₂O₄
• Molecular Weight: 356.75982
• Mol File: 128807-50-1.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: methyl 3-(4-chlorophenyl)-2,5-dioxo-4-phenyl-2,5-dihydro-1H-pyrrol-1-ylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-(4-chlorophenyl)-2,5-dioxo-4-phenyl-2,5-dihydro-1H-pyrrol-1-ylcarbamate(128807-50-1)
• EPA Substance Registry System: methyl 3-(4-chlorophenyl)-2,5-dioxo-4-phenyl-2,5-dihydro-1H-pyrrol-1-ylcarbamate(128807-50-1)

Safety Data

• Hazardous Substances Data: 128807-50-1(Hazardous Substances Data)

Upstream product

• 102862-20-4 3-(4-Chloro-phenyl)-imidazo[1,2-a]pyridin-2-ol 
• 110520-35-9 N'-(2-Bromo-2-phenyl-acetyl)-hydrazinecarboxylic acid methyl ester 

Relevant articles and documents

SYNTHESE DE N-AMINO MALEIMIDES ET D'ANHYDRIDES MALEIQUES DISUBSTITUES A PARTIR D'α-HALOGENO HYDRAZIDES. ETUDE DU MECANISME DE LA REACTION.

α-Halohydrazides react with 2-aminopyridine to give symmetrically substituted N-aminomaleimides.We have shown that this reaction proceeds through the formation of 4-hydroxyimidazopyridines.This result opens a new route to dissymetrically substituted N-aminomaleimides.The hydrolysis of N-aminomaleimides is a grood route to substituted maleic anhydrides.