97253-74-2

Basic information

• Product Name: N,N-dimethyl-3-butenamide
• CAS NO: 97253-74-2
• Molecular Weight: 113.159
• Mol File: 97253-74-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N,N-dimethyl-3-butenamide(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-dimethyl-3-butenamide(97253-74-2)
• EPA Substance Registry System: N,N-dimethyl-3-butenamide(97253-74-2)

Safety Data

• Hazardous Substances Data: 97253-74-2(Hazardous Substances Data)

Upstream product

• 106-95-6 allyl bromide 
• 479486-96-9 N,N-dimethyl (trimethylsilyl)methanamide 
• 854278-29-8 dimethyl-selenocarbamic acid Se-(dimethylcarbamoylselanyl-phenyl-methyl) ester 
• 762-72-1 allyl-trimethyl-silane 

Downstream Products

• 14064-75-6 (E)-N,N-dimethylcrotonamide 
• 97253-81-1 N,N,N',N'-tetramethyl-2-ethenyl-3-methylpentanediamide 
• 97253-76-4 (Z)-N,N-dimethyl-2-butenamide 

Relevant articles and documents

Stannic chloride-induced unsymmetrical C-se bond cleavage of bis(N,N-dimethylcarbamoylseleno)methanes: Novel generation of selenoaldehydes

Treatment of bis(N,N-dimethylcarbamoylseleno)methanes with SnCl4 afforded β-1,3,5-triselenanes in moderate to high yields, and the key intermediates of the reactions, i.e., acylselonium ions and selenoaldehydes, were successfully trapped by usi

Palladium-catalyzed conversion of benzylic and allylic halides into α-aryl and β,γ-unsaturated tertiary amides by the use of a carbamoylsilane

Treatment of allylic and benzylic halides with N,N- dimethylcarbamoyl(trimethyl)silane in the presence of tetrakis- (triphenylphosphine)palladium(0) affords tertiary amides, which arise from the replacement of the halogen by the N,N-dimethylcarbamoyl group.