1567951-64-7

Basic information

• Product Name: 4-(4-methoxyphenyl)-3-(4-nitrophenyl)pyrrole-2-carboxylic acid
• Synonyms: 4-(4-methoxyphenyl)-3-(4-nitrophenyl)pyrrole-2-carboxylic acid
• CAS NO: 1567951-64-7
• Molecular Weight: 338.32
• Mol File: 1567951-64-7.mol

Chemical Properties

• CAS DataBase Reference: 4-(4-methoxyphenyl)-3-(4-nitrophenyl)pyrrole-2-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-methoxyphenyl)-3-(4-nitrophenyl)pyrrole-2-carboxylic acid(1567951-64-7)
• EPA Substance Registry System: 4-(4-methoxyphenyl)-3-(4-nitrophenyl)pyrrole-2-carboxylic acid(1567951-64-7)

Safety Data

• Hazardous Substances Data: 1567951-64-7(Hazardous Substances Data)

Upstream product

• 38335-24-9 3-(4-nitrophenyl)-2-oxopropanoic acid 
• 6303-59-9 (E)-4-(2-bromo-vinyl)-anisole 

Relevant articles and documents

Synthesis of 3,4-diaryl- and 4-acyl-3-arylpyrroles and study of their antimitotic activity

The Barton–Zard reaction of nitro substituted stilbenes and chalcones with ethyl isocyanoacetate afforded 3,4-diaryl- and 4-acyl-3-arylpyrroles, respectively. 3-Arylpyrrole-2,4- dicarboxylates and 4-arylisoxazoline N-oxides were side reaction products. An

A copper-catalyzed coupling reaction of vinyl halides and carbazates: Application in the assembly of polysubstituted pyrroles

CuI-catalyzed coupling of vinyl halides with carbazates gives N-protected N-alkenylhydrazines, which are condensed with ketones under acidic conditions to give polysubstituted pyrroles. The pyrrole synthesis may go through a similar mechanism with Fischer indole synthesis, which involves a [3,3]-sigmatropic rearrangement and other reactions. The Royal Society of Chemistry.