952009-31-3

Basic information

• Product Name: 2-methyl-1,4-diphenyl-1H-pyrrole
• Synonyms: 2-methyl-1,4-diphenyl-1H-pyrrole
• CAS NO: 952009-31-3
• Molecular Weight: 233.313
• Mol File: 952009-31-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-methyl-1,4-diphenyl-1H-pyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methyl-1,4-diphenyl-1H-pyrrole(952009-31-3)
• EPA Substance Registry System: 2-methyl-1,4-diphenyl-1H-pyrrole(952009-31-3)

Safety Data

• Hazardous Substances Data: 952009-31-3(Hazardous Substances Data)

Upstream product

• 82323-38-4 (Z)-5-bromo-4-phenylpent-3-en-2-one 
• 62-53-3 aniline 
• 122-57-6 1-Phenylbut-1-en-3-one 
• 500055-91-4 cyano-2 phenyl-3 oxo-5 hexanoate de methyle 
• 1373319-70-0 methyl 5-methyl-1,3-diphenyl-1H-pyrrole-2-carboxylate 
• 1354642-78-6 methyl 2,5-dioxo-3-phenylhexanoate 
• 5883-81-8 2-anilinoacetophenone 
• 7664-93-9 sulfuric acid 
• 861591-44-8 (2-methyl-1,4-diphenyl-pyrrol-3-yl)-phenyl ketone 
• 155014-69-0 1-(2-methyl-1,4-diphenyl-1H-pyrrol-3-yl)ethanone 

Downstream Products

• 860759-94-0 2,4-diacetyl-5-methyl-1,3-diphenyl-pyrrole 

Relevant articles and documents

γ-halo-enones: A method for their synthesis from arylacyl halides and their application to the preparation of five-membered ring heterocycles

A simple method has been developed for synthesis of γ-halo-enones. The approach employs a sequence involving initial indium-mediated allenylation reactions of phenacyl halides with propargyl bromide. This process is followed by acid-promoted rearrangement reactions of the formed homoallenic halohydrins. The new method can be incorporated into routes for the efficient synthesis of various five-membered heterocyclic compounds.