953395-35-2

Basic information

• Product Name: N-[2-(4-hydroxy-butyl)-phenyl]-4-methyl-benzenesulfonamide
• Synonyms: N-[2-(4-hydroxy-butyl)-phenyl]-4-methyl-benzenesulfonamide
• CAS NO: 953395-35-2
• Molecular Weight: 319.425
• Mol File: 953395-35-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-[2-(4-hydroxy-butyl)-phenyl]-4-methyl-benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[2-(4-hydroxy-butyl)-phenyl]-4-methyl-benzenesulfonamide(953395-35-2)
• EPA Substance Registry System: N-[2-(4-hydroxy-butyl)-phenyl]-4-methyl-benzenesulfonamide(953395-35-2)

Safety Data

• Hazardous Substances Data: 953395-35-2(Hazardous Substances Data)

Upstream product

• 209967-17-9 4-(2-aminophenyl)-1-butanol 
• 98-59-9 p-toluenesulfonyl chloride 
• 881417-15-8 1-(p-toluenesulfonyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one 
• 4424-80-0 2,3,4,5-tetrahydro-1H-1-benzo[b]azepin-2-one 

Downstream Products

• 953395-39-6 4-(2-(4-methylphenylsulfonamido)phenyl)butyl 2-ethynylbenzoate 
• 953395-38-5 4-(2-(4-methylphenylsulfonamido)phenyl)butyl 4-pentynoate 
• 881417-15-8 1-(p-toluenesulfonyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one 
• 20426-63-5 1-(p-Tolylsulfonyl)-2,3,4,5-tetrahydro-1H-1-benzazepine 
• 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

Efficient synthesis of functionalized benzazepine derivatives utilizing intramolecular mitsunobu reaction

The 5-hydroxy-2,3,4,5-tetrahydro-1H-benzazepine derivative (2), which is a typical metabolite of mozavaptan (1) having the 2,3,4,5-tetrahydro-1H-benzazepine skeleton, was synthesized by utilizing the intramolecular Mitsunobu reaction of the corresponding