117794-75-9

Basic information

• Product Name: N-allyl-N-[2-(phenyl)prop-2-en-1-yl]-N-(p-toluenesulfonyl)amide
• Synonyms: N-allyl-N-[2-(phenyl)prop-2-en-1-yl]-N-(p-toluenesulfonyl)amide
• CAS NO: 117794-75-9
• Molecular Weight: 327.447
• Mol File: 117794-75-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-allyl-N-[2-(phenyl)prop-2-en-1-yl]-N-(p-toluenesulfonyl)amide(CAS DataBase Reference)
• NIST Chemistry Reference: N-allyl-N-[2-(phenyl)prop-2-en-1-yl]-N-(p-toluenesulfonyl)amide(117794-75-9)
• EPA Substance Registry System: N-allyl-N-[2-(phenyl)prop-2-en-1-yl]-N-(p-toluenesulfonyl)amide(117794-75-9)

Safety Data

• Hazardous Substances Data: 117794-75-9(Hazardous Substances Data)

Upstream product

• 56865-69-1 N-allyl-2-phenylprop-2-en-1-amine 
• 98-59-9 p-toluenesulfonyl chloride 
• 3360-54-1 3-bromo-2-phenylprop-1-ene 
• 50487-71-3 4-methyl-N-(2-propenyl)benzenesulfonamide 
• 58567-50-3 N-[2-(phenyl)prop-2-en-1-yl]-N-(p-toluenesulfonyl)amide 
• 106-95-6 allyl bromide 
• 5155-87-3 3-phenylbut-3-enoic acid 
• 127-65-1 chloroamine-T 

Downstream Products

• 50487-71-3 4-methyl-N-(2-propenyl)benzenesulfonamide 
• 7283-47-8 (4,4-dimethylpent-1-en-2-yl)benzene 
• 877614-77-2 3-phenyl-1-p-toluenesulfonyl-1,2,5-trihydropyrrole 

Relevant articles and documents

Iodine-Catalyzed Decarboxylative Amidation of β,γ-Unsaturated Carboxylic Acids with Chloramine Salts Leading to Allylic Amides

The iodine-catalyzed decarboxylative amidation of β,γ-unsaturated carboxylic acids with chloramine salts is described. This method enables the regioselective synthesis of allylic amides from various types of β,γ-unsaturated carboxylic acids containing sub

2-Arylallyl as a new protecting group for amines, amides and alcohols

Amines, amides and ethers containing 2-arylallyl groups are selectively and easily deprotected with tert-butyllithium. This transformation probably involves a carbolithiation reaction of the styrenyl moiety followed by a β-elimination process. The Royal Society of Chemistry 2005.