1330574-07-6

Basic information

• Product Name: (5-(4-toluenesulfonyl)-5,6-dihydrophenanthridine-6-yl)propan-2-one
• Synonyms: (5-(4-toluenesulfonyl)-5,6-dihydrophenanthridine-6-yl)propan-2-one
• CAS NO: 1330574-07-6
• Molecular Weight: 391.491
• Mol File: 1330574-07-6.mol

Chemical Properties

• CAS DataBase Reference: (5-(4-toluenesulfonyl)-5,6-dihydrophenanthridine-6-yl)propan-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (5-(4-toluenesulfonyl)-5,6-dihydrophenanthridine-6-yl)propan-2-one(1330574-07-6)
• EPA Substance Registry System: (5-(4-toluenesulfonyl)-5,6-dihydrophenanthridine-6-yl)propan-2-one(1330574-07-6)

Safety Data

• Hazardous Substances Data: 1330574-07-6(Hazardous Substances Data)

Upstream product

• 90-41-5 2-phenylaniline 
• 98-59-9 p-toluenesulfonyl chloride 
• 72454-54-7 4-(2-bromophenyl)but-3-en-2-one 
• 796061-07-9 4-methyl-N-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzenesulfonamide 
• 440084-09-3 4-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)but-3-en-2-one 
• 1024-38-0 N-(2-bromophenyl)-4-methylbenzenesulfonamide 
• 24310-30-3 N-biphenyl-2-yl-4-methylbenzenesulfonamide 
• 78-94-4 methyl vinyl ketone 

Relevant articles and documents

Synthesis of 6-Substituted Phenanthridine Derivatives by Palladium-Catalysed Domino Suzuki-Miyaura/Aza-Michael Reactions

An efficient method for the synthesis of 6-substituted phenanthridine derivatives has been developed through a one-pot process involving a sequence of palladium-catalysed Suzuki-Miyaura reaction followed by intramolecular aza-Michael addition. This method is applicable to the synthesis of a wide range of substituted phenanthridines from simple substrates.

Pd-catalyzed sequential C-C and C-N bond formations for the synthesis of N-heterocycles: Exploiting protecting group-directed C-H activation under modified reaction conditions

Easy & efficient: A Pd-catalyzed domino olefination/conjugate addition reaction of N-Ts-2-arylanilines with activated olefins has been achieved at ambient temperature under the newly defined reaction conditions. This process highlighted the directing effect of the N-protecting group in C-H activation, displayed broad substrate scope with wide functional group compatibility; thus rendering a straightforward entry to a wide variety of N-heterocycles such as dihydrophenanthridines.