881417-15-8

Basic information

• Product Name: 1-(p-toluenesulfonyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one
• Synonyms: 1-(p-toluenesulfonyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one
• CAS NO: 881417-15-8
• Molecular Weight: 315.393
• Mol File: 881417-15-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-(p-toluenesulfonyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(p-toluenesulfonyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one(881417-15-8)
• EPA Substance Registry System: 1-(p-toluenesulfonyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one(881417-15-8)

Safety Data

• Hazardous Substances Data: 881417-15-8(Hazardous Substances Data)

Upstream product

• 4424-80-0 2,3,4,5-tetrahydro-1H-1-benzo[b]azepin-2-one 
• 98-59-9 p-toluenesulfonyl chloride 
• 209967-17-9 4-(2-aminophenyl)-1-butanol 
• 953395-35-2 N-[2-(4-hydroxy-butyl)-phenyl]-4-methyl-benzenesulfonamide 

Downstream Products

• 953395-35-2 N-[2-(4-hydroxy-butyl)-phenyl]-4-methyl-benzenesulfonamide 
• 881417-13-6 N-[2-(4-hydroxypentyl)phenyl]-p-toluenesulfonamide 

Relevant articles and documents

Biomimetic aerobic oxidation of amino alcohols to lactams

The right path: N-Protected amino alcohols undergo aerobic and biomimetic oxidation to the corresponding lactams in the presence of a ruthenium catalyst and a combination of electron-transfer mediators under air (see scheme). The reaction was used for the synthesis of five-, six-, and seven-, membered lactams and showed good tolerance to a number of N-protecting groups. Copyright