66236-05-3

Basic information

• Product Name: Benzenesulfonamide, 4-methyl-N-(4-methylphenyl)-N-2-propenyl-
• CAS NO: 66236-05-3
• Molecular Formula: C17H19NO2S
• Molecular Weight: 301.409
• Mol File: 66236-05-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, 4-methyl-N-(4-methylphenyl)-N-2-propenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, 4-methyl-N-(4-methylphenyl)-N-2-propenyl-(66236-05-3)
• EPA Substance Registry System: Benzenesulfonamide, 4-methyl-N-(4-methylphenyl)-N-2-propenyl-(66236-05-3)

Safety Data

• Hazardous Substances Data: 66236-05-3(Hazardous Substances Data)

Upstream product

• 4743-74-2 2-phenylpent-4-en-2-ol 
• 599-86-0 4-methyl-N-(4-methylphenyl)benzenesulfonamide 
• 106-95-6 allyl bromide 
• 15258-46-5 N-allyl-p-toluidine 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 1443775-63-0 N-(2-fluoropropyl)-N-(4-methylphenyl)-4-methylbenzenesulfonamide 

Relevant articles and documents

Palladium-Catalyzed Allylic Amination of Homoallylic Alcohols with Amines via Carbon-Carbon Bond Cleavage

An efficient approach for palladium(II) acetate catalyzed allylic amination of homoallylic alcohols with various amines via sequential retro-allylation and amination was developed, which afforded the corresponding allylic amines in up to 98% yield.

Synthesis of highly substituted dibenzoazocine derivatives by the aza-Claisen rearrangement and intramolecular Heck reaction via 8-exo-trig mode of cyclization

The synthesis of highly substituted dibenzo-azocine systems is still lacking. An efficient synthetic protocol utilizing the sequential aromatic aza-Claisen rearrangement followed by the implementation of the intramolecular Heck reaction as a key step has been developed for the synthesis of various dibenzo-azocine derivatives of biological relevance.