96757-78-7

Basic information

• Product Name: Ethanone, 1-(2-methyl-1,5-diphenyl-1H-pyrrol-3-yl)-
• CAS NO: 96757-78-7
• Molecular Formula: C19H17NO
• Molecular Weight: 275.35
• Mol File: 96757-78-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-(2-methyl-1,5-diphenyl-1H-pyrrol-3-yl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(2-methyl-1,5-diphenyl-1H-pyrrol-3-yl)-(96757-78-7)
• EPA Substance Registry System: Ethanone, 1-(2-methyl-1,5-diphenyl-1H-pyrrol-3-yl)-(96757-78-7)

Safety Data

• Hazardous Substances Data: 96757-78-7(Hazardous Substances Data)

Upstream product

• 62-53-3 aniline 
• 70-11-1 α-bromoacetophenone 
• 123-54-6 acetylacetone 
• 95-54-5 1,2-diamino-benzene 
• 52313-43-6 3-acetyl-1-phenyl-pentane-1,4-dione 
• 3771-57-1 2-methyl-1,5-diphenyl-1H-pyrrole 
• 75-36-5 acetyl chloride 
• 109662-94-4 1-[1-(2-Amino-phenyl)-2-methyl-5-phenyl-1H-pyrrol-3-yl]-ethanone 
• 96757-84-5 3-phenacylacetylacetone 

Downstream Products

• 109811-56-5 2-hydroxy-1-(2-methyl-1,5-diphenyl-pyrrol-3-yl)-ethanone 
• 109693-68-7 (2-methyl-1,5-diphenyl-pyrrol-3-yl)-glyoxylonitrile 
• 109812-64-8 2-methyl-1,5-diphenyl-pyrrole-3-carboxylic acid 
• 96757-80-1 1-(2-Methyl-1,5-diphenyl-1H-pyrrol-3-yl)-ethanol 
• 130870-94-9 1-(4-Bromo-2-methyl-1,5-diphenyl-1H-pyrrol-3-yl)-ethanone 
• 105357-87-7 (E)-α-1,5-diphenyl-3-pyrrylethylidene(isopropylidene)succinic anhydride 
• 109806-81-7 (2-methyl-1,5-diphenyl-pyrrol-3-yl)-glyoxal 
• 102949-25-7 1-(2-methyl-1,5-diphenyl-pyrrol-3-yl)-3t-phenyl-propenone 

Relevant articles and documents

Multicomponent approach towards the synthesis of substituted pyrroles under supramolecular catalysis using β-cyclodextrin as a catalyst in water under neutral conditions

Synthesis of substituted pyrroles in H2O by using β-cyclodextrin as a supramolecular catalyst is described. This reaction has several advantages over existing methods and provides substituted pyrroles in good-to-excellent yields (79-89%). The s

POLYCONDENSED NITROGEN HETEROCYCLES. PART 20. REACTIVITY OF DIAZOTIZED 1-(2-AMINOPHENYL)-PYRROLES. PYRROLOPHENANTHRIDINES

Compounds (2) were diazotized under several conditions to prepare pyrrolophenanthridines (5).However, together with the Pschorr type cyclization, decomposition and intermolecular coupling reactions were observed.