79402-71-4

Basic information

• Product Name: N-(α-ethylbenzylidene)acetamide
• Synonyms: N-(α-ethylbenzylidene)acetamide
• CAS NO: 79402-71-4
• Molecular Weight: 175.23
• Mol File: 79402-71-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(α-ethylbenzylidene)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(α-ethylbenzylidene)acetamide(79402-71-4)
• EPA Substance Registry System: N-(α-ethylbenzylidene)acetamide(79402-71-4)

Safety Data

• Hazardous Substances Data: 79402-71-4(Hazardous Substances Data)

Upstream product

• 100-47-0 benzonitrile 
• 16205-14-4 2-phenyl-3-methylazirine 
• 52755-67-6 2-methyl-4-phenyl-Δ³-oxazolinone 
• 4855-25-8 2-methyl-4-ethyl-4-phenyl-Δ²-oxazolin-5-one 
• 93-54-9 1-Phenyl-1-propanol 
• 60059-18-9 acetyl isopropyl carbonate 
• 29076-84-4 propiophenone-imine 
• 75-36-5 acetyl chloride 
• 925-90-6 ethylmagnesium bromide 

Downstream Products

• 1575-95-7 N-acetylbenzamide 
• 7664-41-7 ammonia 
• 64-19-7 acetic acid 
• 93-55-0 1-phenyl-propan-1-one 
• 495-40-9 propiophenone 

Relevant articles and documents

Chemoselective, Isomerization-Free Synthesis of N-Acylketimines from N–H Imines

N-Acylketimines were synthesized through a ruthenium-catalyzed generation of N–H ketimines from secondary azides and subsequent acylation with mixed anhydrides under mild conditions. The synthetic scope was broad to give N-acylimines having various functi

SIGMATROPIC REARRANGEMENTS IN THE ALLYL SUBSTITUTED OXAZOLINONE SYSTEM

Thermolysis and photolysis of several allyl substituted oxazolin-5-ones results in a sigmatropic rearrangement in accord with orbital symmetry predictions.