128588-63-6

Basic information

• Product Name: 2,3-Diphenyl-5-(3-methoxyphenyl)pyrrole
• Synonyms: 2,3-Diphenyl-5-(3-methoxyphenyl)pyrrole
• CAS NO: 128588-63-6
• Molecular Weight: 325.41
• Mol File: 128588-63-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,3-Diphenyl-5-(3-methoxyphenyl)pyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-Diphenyl-5-(3-methoxyphenyl)pyrrole(128588-63-6)
• EPA Substance Registry System: 2,3-Diphenyl-5-(3-methoxyphenyl)pyrrole(128588-63-6)

Safety Data

• Hazardous Substances Data: 128588-63-6(Hazardous Substances Data)

Upstream product

• 16483-98-0 2,3-diphenyl-2H-azirine 
• 349537-50-4 N-(1-(3-methoxyphenyl)vinyl)acetamide 
• 122806-25-1 1-(3-methoxy-phenyl)-ethanone oxime 
• 586-37-8 1-(3-Methoxyphenyl)ethanone 
• 501-65-5 diphenyl acetylene 
• 119-53-9 2-hydroxy-2-phenylacetophenone 

Downstream Products

• 128588-65-8 2,3-Diphenyl-5-(3-methoxyphenyl)-4-nitrosopyrrole 

Relevant articles and documents

Iron-Catalyzed Radical Cycloaddition of 2H-Azirines and Enamides for the Synthesis of Pyrroles

A novel and efficient Fe-catalyzed radical cycloaddition of 2H-azirines and enamides for the synthesis of substituted pyrroles has been developed. The radical cycloaddition reaction proceeded through a conceptually new Fe(II)-catalyzed homolytic cleavage of C-N bond of 2H-azirines sequential radical cyclization with enamides. The reaction used readily available starting materials, tolerated various functional groups, and afforded valuable triaryl-substituted pyrroles in good to high yields under mild reaction conditions.

ortho Effect on the Nitrosation of the 2,3-Diphenyl-5-(2-methoxyphenyl)pyrrole

A comparison of the behaviour on the nitrosation of the isomers 5-(2-methoxyphenyl)- (1a), 5-(3-methoxyphenyl)- (1b) and 5-(4-methoxyphenyl)-2,3-diphenylpyrroles (1c) carried out in the usual way with iso-amyl nitrite in a solution of sodium ethoxide in e