1263146-01-5

Basic information

• Product Name: 7-chloro-1,3,3,9-tetraphenyl-3H-pyrrolo[1,2-a]indole
• Synonyms: 7-chloro-1,3,3,9-tetraphenyl-3H-pyrrolo[1,2-a]indole
• CAS NO: 1263146-01-5
• Molecular Weight: 494.035
• Mol File: 1263146-01-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 7-chloro-1,3,3,9-tetraphenyl-3H-pyrrolo[1,2-a]indole(CAS DataBase Reference)
• NIST Chemistry Reference: 7-chloro-1,3,3,9-tetraphenyl-3H-pyrrolo[1,2-a]indole(1263146-01-5)
• EPA Substance Registry System: 7-chloro-1,3,3,9-tetraphenyl-3H-pyrrolo[1,2-a]indole(1263146-01-5)

Safety Data

• Hazardous Substances Data: 1263146-01-5(Hazardous Substances Data)

Upstream product

• 22072-89-5 5-Chloro-3-phenyl-1H-indole 
• 1522-13-0 1,1,3-triphenylprop-2-yn-1-ol 

Relevant articles and documents

Chemoselective cascade synthesis of N-fused heterocycles via silver(I) triflate-catalyzed friedel-crafts/N-C bond formation sequence

An efficient cascade methodology toward chemoselective synthesis of N-fused heterocycles including 9H-pyrrolo[1,2-a]indole, 3H-pyrrolo[1,2-a]indole and 1H-pyrrolo[1,2-a]indole derivatives has been developed. This transformation proceeds via a silver(I) triflate-catalyzed consecutive Friedel-Crafts reaction/N-C bond formation sequence between readily available propargyl alcohols and 3-substituted 1H-indoles. Not only is excellent chemoselectivity observed according to the substitution patterns of propargyl alcohols, but also the Lewis acid-catalyzed N-C bond formation process can be carried out under base- and ligand-free conditions. Copyright