3274-66-6

Basic information

• Product Name: ethyl 2,4,5-triphenyl-1H-pyrrole-3-carboxylate
• Synonyms: ethyl 2,4,5-triphenyl-1H-pyrrole-3-carboxylate
• CAS NO: 3274-66-6
• Molecular Weight: 367.447
• Mol File: 3274-66-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: ethyl 2,4,5-triphenyl-1H-pyrrole-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2,4,5-triphenyl-1H-pyrrole-3-carboxylate(3274-66-6)
• EPA Substance Registry System: ethyl 2,4,5-triphenyl-1H-pyrrole-3-carboxylate(3274-66-6)

Safety Data

• Hazardous Substances Data: 3274-66-6(Hazardous Substances Data)

Upstream product

• 53256-19-2 ethyl (Z)-3-amino-3-phenylacrylate 
• 115080-52-9 (2,4,5-triphenyl-pyrrol-3-yl)-glyoxal-2-oxime 
• 112323-17-8 (2,4,5-triphenyl-pyrrol-3-yl)-glyoxylonitrile 
• 100-52-7 benzaldehyde 
• 15341-31-8 α-nitro-stilbene 
• 105-36-2 ethyl bromoacetate 
• 100-47-0 benzonitrile 

Downstream Products

• 3274-61-1 2,4,5-triphenylpyrrole 
• 98304-68-8 2,4,5-triphenyl-pyrrole-3-carboxylic acid 

Relevant articles and documents

Catalyst-Dependent Chemoselective Formal Insertion of Diazo Compounds into C?C or C?H Bonds of 1,3-Dicarbonyl Compounds

A catalyst-dependent chemoselective one-carbon insertion of diazo compounds into the C?C or C?H bonds of 1,3-dicarbonyl species is reported. In the presence of silver(I) triflate, diazo insertion into the C(=O)?C bond of the 1,3-dicarbonyl substrate leads

Iron-catalyzed tandem one-pot addition and cyclization of the blaise reaction intermediate and nitroolefins: Synthesis of substituted NH-pyrroles from nitriles

The iron-catalyzed addition and cyclization of the Blaise reaction intermediate and nitroolefins to synthesize highly functionalized NH-pyrroles in a tandem one-pot manner from nitriles has been developed. This reaction shows good functional group tolerance and affords a broad spectrum of substituted NH-pyrroles in good yields. Copyright