1292302-62-5

Basic information

• Product Name: N-(2-phenylbenzylidene)-4-methylbenzenesulfonamide
• Synonyms: N-(2-phenylbenzylidene)-4-methylbenzenesulfonamide
• CAS NO: 1292302-62-5
• Molecular Weight: 335.426
• Mol File: 1292302-62-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-(2-phenylbenzylidene)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-phenylbenzylidene)-4-methylbenzenesulfonamide(1292302-62-5)
• EPA Substance Registry System: N-(2-phenylbenzylidene)-4-methylbenzenesulfonamide(1292302-62-5)

Safety Data

• Hazardous Substances Data: 1292302-62-5(Hazardous Substances Data)

Upstream product

• 1203-68-5 2-Phenylbenzaldehyde 
• 4083-64-1 Tosyl isocyanate 
• 98-80-6 phenylboronic acid 
• 6630-33-7 ortho-bromobenzaldehyde 
• 70-55-3 toluene-4-sulfonamide 

Downstream Products

• 94623-63-9 N-(9H-fluoren-9-yl)-4-methylbenzenesulfonamide 
• 1203-68-5 2-Phenylbenzaldehyde 
• 486-25-9 9-fluorenone 

Relevant articles and documents

Synthesis of N-Sulfonyl Arylaldimines Developed by Retesting an Old Process

By simply heating the mixture of an arylaldehyde and a sulfonylisocyanate in a solvent or in neat form under catalyst- and additive-free conditions, the desired N-sulfonylimine was produced with the release of carbon dioxide. The method is characterized b

Efficient synthesis of 9-tosylaminofluorene derivatives by boron trifluoride etherate-catalyzed aza-friedel-crafts reaction of in situ generated N-tosylbenzaldimines

An efficient and expeditious boron trifluoride etherate (BF 3·Et2O) catalyzed one-pot reaction for the synthesis of N-tosyl-9-aminofluorenes and anthracene derivatives from in situ generated N-tosylbenzaldimines via an aza-Friedal-Crafts reaction has been developed. The catalytic reaction shows high substrate tolerance with excellent yields.