1269261-57-5

Basic information

• Product Name: N-(2-(but-3-en-1-yl)-6-chlorophenyl)-4-methylbenzenesulfonamide
• Synonyms: N-(2-(but-3-en-1-yl)-6-chlorophenyl)-4-methylbenzenesulfonamide
• CAS NO: 1269261-57-5
• Molecular Weight: 335.854
• Mol File: 1269261-57-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-(2-(but-3-en-1-yl)-6-chlorophenyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-(but-3-en-1-yl)-6-chlorophenyl)-4-methylbenzenesulfonamide(1269261-57-5)
• EPA Substance Registry System: N-(2-(but-3-en-1-yl)-6-chlorophenyl)-4-methylbenzenesulfonamide(1269261-57-5)

Safety Data

• Hazardous Substances Data: 1269261-57-5(Hazardous Substances Data)

Upstream product

• 1252576-11-6 N-(2-chloro-6-(chloromethyl)phenyl)-4-methylbenzenesulfonamide 
• 2622-05-1 allylmagnesium bromide 
• 98-59-9 p-toluenesulfonyl chloride 
• 1252576-10-5 N-(6-chloro-2-(hydroxymethyl)phenyl)-4-methylbenzenesulfonamide 
• 61487-25-0 (2-amino-3-chlorophenyl)methanol 

Downstream Products

• 1269261-75-7 2-(bromomethyl)-8-chloro-1-(toluene-4-sulfonyl)-1,2,3,4-tetrahydroquinoline 
• 1421826-94-9 (8-chloro-1-tosyl-1,2,3,4-tetrahydroquinolin-2-yl)-methyl acetate 

Relevant articles and documents

Palladium(II)-catalyzed aerobic intramolecular allylic C[sbnd]H activation for the synthesis of indolines

A method for the preparation of indolines via palladium-catalyzed aerobic intramolecular allylic C[sbnd]H activation was developed. Oxygen was successfully used as oxidant with catalytic amount of 1,4-benzoquinone. 16 examples were reported, the majority of substrates gave moderate to good yields.