1383950-50-2

Basic information

• Product Name: N-((3S,4S)-3-hydroxy-1,3-diphenylhept-1-yn-4-yl)-4-methylbenzenesulfonamide
• CAS NO: 1383950-50-2
• Molecular Weight: 433.571
• Mol File: 1383950-50-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-((3S,4S)-3-hydroxy-1,3-diphenylhept-1-yn-4-yl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-((3S,4S)-3-hydroxy-1,3-diphenylhept-1-yn-4-yl)-4-methylbenzenesulfonamide(1383950-50-2)
• EPA Substance Registry System: N-((3S,4S)-3-hydroxy-1,3-diphenylhept-1-yn-4-yl)-4-methylbenzenesulfonamide(1383950-50-2)

Safety Data

• Hazardous Substances Data: 1383950-50-2(Hazardous Substances Data)

Upstream product

• 536-74-3 phenylacetylene 

Downstream Products

• 1383950-73-9 (3S,4S)-4-(4-methylphenylsulfonamido)-1,3-diphenylhept-1-yn-3-yl benzoate 
• 1427520-28-2 ((3R,6S)-3-methyl-5-phenyl-6-propyl-1-tosyl-1,2,3,6-tetrahydropyridin-4-yl)(phenyl)methanone 
• 1427520-14-6 2-((3R,6S)-4-benzoyl-5-phenyl-6-propyl-1-tosyl-1,2,3,6-tetrahydropyridin-3-yl)-1-cyclopropylethanone 
• 1427519-95-6 (3S,4S)-4-(N-allyl-4-methylphenylsulfonamido)-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.