250695-13-7

Basic information

• Product Name: (p-tolyl)[5-(p-toluoyl)furan-2-yl][5-(p-toluoyl)pyrrol-2-yl]methane
• Synonyms: (p-tolyl)[5-(p-toluoyl)furan-2-yl][5-(p-toluoyl)pyrrol-2-yl]methane
• CAS NO: 250695-13-7
• Molecular Weight: 473.571
• Mol File: 250695-13-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (p-tolyl)[5-(p-toluoyl)furan-2-yl][5-(p-toluoyl)pyrrol-2-yl]methane(CAS DataBase Reference)
• NIST Chemistry Reference: (p-tolyl)[5-(p-toluoyl)furan-2-yl][5-(p-toluoyl)pyrrol-2-yl]methane(250695-13-7)
• EPA Substance Registry System: (p-tolyl)[5-(p-toluoyl)furan-2-yl][5-(p-toluoyl)pyrrol-2-yl]methane(250695-13-7)

Safety Data

• Hazardous Substances Data: 250695-13-7(Hazardous Substances Data)

Upstream product

• 224962-61-2 2-[α-hydroxy-α-(p-tolyl)]methylfuran 
• 874-60-2 4-methyl-benzoyl chloride 
• 250695-05-7 (p-tolyl)(furan-2-yl)(pyrrol-2-yl)methane 

Downstream Products

• 250695-24-0 (5-{[5-(hydroxy-p-tolyl-methyl)-1H-pyrrol-2-yl]-p-tolyl-methyl}-furan-2-yl)-p-tolyl-methanol 

Relevant articles and documents

Customized, core-modified corroles from [2+2] condensation of dipyrromethanes

Corroles and core-modified corroles were synthesized by acid-catalyzed condensation under low-scrambling conditions. The synthesis utilized [2+2] condensation of two different dipyrromethanes. The condensation afforded different corroles bearing heteroatoms in a predesignated location depending on the starting dipyrromethanes. Selective α-α' linkage was achieved by positioning a linking carbon unit at a different site of dipyrromethanes. (C) 2000 Elsevier Science Ltd.