1383950-52-4

Basic information

• Product Name: N-((3S,4S)-3-hydroxy-6-methyl-1,3-diphenylhept-1-yn-4-yl)-4-methylbenzenesulfonamide
• CAS NO: 1383950-52-4
• Molecular Weight: 447.598
• Mol File: 1383950-52-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-((3S,4S)-3-hydroxy-6-methyl-1,3-diphenylhept-1-yn-4-yl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-((3S,4S)-3-hydroxy-6-methyl-1,3-diphenylhept-1-yn-4-yl)-4-methylbenzenesulfonamide(1383950-52-4)
• EPA Substance Registry System: N-((3S,4S)-3-hydroxy-6-methyl-1,3-diphenylhept-1-yn-4-yl)-4-methylbenzenesulfonamide(1383950-52-4)

Safety Data

• Hazardous Substances Data: 1383950-52-4(Hazardous Substances Data)

Upstream product

• 1383950-31-9 (S)-4-methyl-N-(4-methyl-1-oxo-1-phenylpentan-2-yl)benzenesulfonamide 
• 536-74-3 phenylacetylene 

Downstream Products

• 1383950-75-1 (3S,4S)-6-methyl-4-(4-methylphenylsulfonamido)-1,3-diphenylhept-1-yn-3-yl benzoate 
• 1427520-27-1 ((3R,6S)-6-isobutyl-3-methyl-5-phenyl-1-tosyl-1,2,3,6-tetrahydropyridin-4-yl)(phenyl)methanone 
• 1427520-18-0 2-((3R,6S)-4-benzoyl-6-isobutyl-5-phenyl-1-tosyl-1,2,3,6-tetrahydropyridin-3-yl)-1-cyclobutylethanone 
• 1427520-15-7 2-((3R,6S)-4-benzoyl-6-isobutyl-5-phenyl-1-tosyl-1,2,3,6-tetrahydropyridin-3-yl)-1-cyclopropylethanone 
• 1427520-08-8 1-((3R,6S)-4-benzoyl-6-isobutyl-5-phenyl-1-tosyl-1,2,3,6-tetrahydropyridin-3-yl)propan-2-one 
• 1427519-89-8 (3S,4S)-4-(N-allyl-4-methylphenylsulfonamido)-6-methyl-1,3-diphenylhept-1-yn-3-yl acetate 
• 1427519-99-0 (3S,4S)-4-(N-allyl-4-methylphenylsulfonamido)-6-methyl-1,3-diphenylhept-1-yn-3-yl cyclobutanecarboxylate 
• 1427519-96-7 (3S,4S)-4-(N-allyl-4-methylphenylsulfonamido)-6-methyl-1,3-diphenylhept-1-yn-3-yl cyclopropanecarboxylate 

Relevant articles and documents

Gold-catalyzed cycloisomerization of 1,7-diyne benzoates to indeno[1,2-c]azepines and azabicyclo[4.2.0]octa-1(8),5-dines

A synthetic method that relies on Au(I)-catalyzed cycloisomerization reactions of 1,7-diyne benzoates to prepare indeno[1,2-c]azepines and azabicyclo[4.2.0]octa-1(8),5-dines is described.