1238251-77-8

Basic information

• Product Name: N-(2-(1-hydroxy-1,3-diphenylprop-2-yn-1-yl)phenyl)-4-methylbenzenesulfonamide
• Synonyms: N-(2-(1-hydroxy-1,3-diphenylprop-2-yn-1-yl)phenyl)-4-methylbenzenesulfonamide
• CAS NO: 1238251-77-8
• Molecular Weight: 453.562
• Mol File: 1238251-77-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-(2-(1-hydroxy-1,3-diphenylprop-2-yn-1-yl)phenyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-(1-hydroxy-1,3-diphenylprop-2-yn-1-yl)phenyl)-4-methylbenzenesulfonamide(1238251-77-8)
• EPA Substance Registry System: N-(2-(1-hydroxy-1,3-diphenylprop-2-yn-1-yl)phenyl)-4-methylbenzenesulfonamide(1238251-77-8)

Safety Data

• Hazardous Substances Data: 1238251-77-8(Hazardous Substances Data)

Upstream product

• 1859-71-8 2-(tosylamino)benzophenone 
• 536-74-3 phenylacetylene 
• 5176-12-5 (2-nitrophenyl)phenylmethanol 
• 340696-10-8 2-(hydroxy(phenyl)methyl)-1-(4-methylphenylsulfonamido)benzene 
• 13209-38-6 (2-aminophenyl)(phenyl)methanol 
• 2835-77-0 (2-aminophenyl)(phenyl)methanone 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 1238252-38-4 (Z)-2-benzylidene-3-phenyl-1-tosylindolin-3-ol 
• 10380-73-1 2,3,4-triphenyl quinoline 
• 1291080-13-1 (E)-ethyl 3-(2,4-diphenylquinolin-3-yl)acrylate 
• 1291080-12-0 2,4-diphenyl-3-(phenylethynyl)quinoline 
• 1238252-33-9 (E)-4-methyl-N-(2-(3-oxo-1,3-diphenylprop-1-enyl)phenyl)benzenesulfonamide 
• 1238252-30-6 6-phenyl-5-tosyl-5,6-dihydroindeno[2,1-b]indole 

Relevant articles and documents

Synthesis of polysubstituted cyclopenta[b]indoles via relay gold(i)/Bronsted acid catalysis

An efficient relay catalytic process involving Au(i)/Bronsted acid to access various polysubstituted cyclopentannulated indoles from easily accessible 1-(2-aminophenyl)prop-2-ynols and readily available 1,3-dicarbonyls has been developed. In an unprecedented event, the intermediate 2-indolylmethyl cations undergo the cation-Ene reaction with various 1,3-dicarbonyls followed by an intramolecular Friedel-Crafts-type reaction generating functionalized cyclopenta[b]indoles. This journal is

Electrophile-driven regioselective synthesis of functionalized quinolines

Highly substituted 3-iodoquinolines bearing different alkyl and aryl moieties can be synthesized in moderate to excellent yields (up to 99%) by 6-endo-dig iodocyclization of 2-tosylaminophenylprop-1-yn-3-ols with molecular iodine (I2) under mil