20886-47-9

Basic information

• Product Name: N,3-dimethyl-N-phenylbut-2-enamide
• Synonyms: N,3-dimethyl-N-phenylbut-2-enamide
• CAS NO: 20886-47-9
• Molecular Weight: 189.257
• Mol File: 20886-47-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N,3-dimethyl-N-phenylbut-2-enamide(CAS DataBase Reference)
• NIST Chemistry Reference: N,3-dimethyl-N-phenylbut-2-enamide(20886-47-9)
• EPA Substance Registry System: N,3-dimethyl-N-phenylbut-2-enamide(20886-47-9)

Safety Data

• Hazardous Substances Data: 20886-47-9(Hazardous Substances Data)

Upstream product

• 3350-78-5 3,3-Dimethylacryloyl chloride 
• 100-61-8 N-methylaniline 
• 34876-10-3 3-methyl-2-butenoic anhydride 
• 121-69-7 N,N-dimethyl-aniline 
• 541-47-9 3-Methylbutenoic acid 
• 139-02-6 sodium phenoxide 
• 108-88-3 toluene 

Downstream Products

• 58461-27-1 (+/-)-lavandulol 
• 20886-50-4 N,3-Dimethyl-2,3-epoxybutananilide 
• 104643-26-7 N,N-diisopropyl-10-methyl-8-oxoundeca-1,5,9-triene-6-carboxamide 
• 104663-58-3 2-(3'-butenyl)-N,N-diisopropyl-N'-phenyl-N',4,4-trimethyl-1,3-cyclopentanedicarboxamide 
• 104643-16-5 2-(3'-butenyl)-N,N-diisopropyl-N'-phenyl-N',3,3-trimethyl-1,4-cyclopentanedicarboxamide 
• 104643-06-3 2-Eth-(E)-ylidene-4,4-dimethyl-hexanedioic acid 1-diisopropylamide 6-(methyl-phenyl-amide) 
• 104643-05-2 (1R,3S,5S)-4,4,5-Trimethyl-cyclopentane-1,3-dicarboxylic acid 1-diisopropylamide 3-(methyl-phenyl-amide) 
• 67986-78-1 N,5-dimethyl-N-phenyl-2-isopropenyl-4-hexenamide 
• 10229-37-5 N-(3-methylbut-2-enyl)-N-methylaniline 

Relevant articles and documents

Synthesis of hydroxyl-containing oxindoles and 3,4-dihydroquinolin-2-ones through oxone-mediated cascade arylhydroxylation of activated alkenes

Hydroxyl-containing compounds are highly value-Added organic molecules, and the establishment of novel methodologies for their elaboration is a long-standing challenge in organic synthesis. Here the first oxone-mediated direct arylhydroxylation of activat

On the preparation of amine N-oxides by using dioxiranes

The reaction of heterocyclic aromatic amines, anilines and tertiary amines with dimethyldioxirane (DMD) was examined. Treatment of heterocyclic aromatic amines and anilines with a slight excess of DMD at 0°C afforded the corresponding N-oxides in quantitative conversion yields. In addition, the oxidation was chemoselective in the presence of carbon-carbon double bonds. On the other hand, most of the tertiary amines assayed did afford also quantitative yields of the corresponding N. oxides, although reaction conditions, in particular regarding the amount of DMD required, depended on each substrate. Additional studies carried out on selected substrates suggested that certain N-oxides derived from tertiary amines deactivate DMD.