77167-05-6

Basic information

• Product Name: N-[2-(allyloxy)phenyl]-4-methylbenzenesulfonamide
• Synonyms: N-[2-(allyloxy)phenyl]-4-methylbenzenesulfonamide
• CAS NO: 77167-05-6
• Molecular Formula: C₁₆H₁₇NO₃S
• Molecular Weight: 303.37608
• Mol File: 77167-05-6.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-[2-(allyloxy)phenyl]-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[2-(allyloxy)phenyl]-4-methylbenzenesulfonamide(77167-05-6)
• EPA Substance Registry System: N-[2-(allyloxy)phenyl]-4-methylbenzenesulfonamide(77167-05-6)

Safety Data

• Hazardous Substances Data: 77167-05-6(Hazardous Substances Data)

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 27096-64-6 2-(allyloxy)aniline 
• 95-55-6 2-amino-phenol 

Downstream Products

• 77167-13-6 N-(2-Allyloxy-phenyl)-4-methyl-N-oxiranylmethyl-benzenesulfonamide 
• 473556-42-2 N-allyl-N-[2-(allyloxy)phenyl]-4-methylbenzenesulfonamide 
• 77176-37-5 N-(2-Allyloxy-phenyl)-N-[2-hydroxy-3-(3-phenyl-propylamino)-propyl]-4-methyl-benzenesulfonamide; compound with oxalic acid 
• 77166-16-6 N-(2-Allyloxy-phenyl)-N-[2-hydroxy-3-(4-pyridin-2-yl-piperazin-1-yl)-propyl]-4-methyl-benzenesulfonamide; compound with oxalic acid 
• 77166-19-9 N-(2-Allyloxy-phenyl)-N-{3-[4-(3-chloro-phenyl)-piperazin-1-yl]-2-hydroxy-propyl}-4-methyl-benzenesulfonamide; compound with oxalic acid 
• 77174-41-5 N-(2-Allyloxy-phenyl)-N-{3-[4-(4-chloro-phenyl)-piperazin-1-yl]-2-hydroxy-propyl}-4-methyl-benzenesulfonamide; compound with oxalic acid 
• 77166-24-6 N-(2-Allyloxy-phenyl)-N-{2-hydroxy-3-[4-(2-methoxy-phenyl)-piperazin-1-yl]-propyl}-4-methyl-benzenesulfonamide; compound with oxalic acid 
• 1253594-74-9 C₁₆H₁₆INO₃S 

Relevant articles and documents

Intramolecular Aminoazidation of Unactivated Terminal Alkenes by Palladium-Catalyzed Reactions with Hydrogen Peroxide as the Oxidant

The palladium-catalyzed aminoazidation of aminoalkenes yielding azidomethyl-substituted nitrogen-containing heterocycles was developed. The procedure requires oxidative conditions and occurs at room temperature in the presence of hydrogen peroxide and NaN3 as the azide source. These conditions provide selective exo-cyclization/azidation of the carbon-carbon double bond, furnishing a versatile approach toward five-, six-, and seven-membered heterocyclic rings.