20428-67-5

Basic information

• Product Name: Benzenepropanamide, b-hydroxy-N,N-dimethyl-b-phenyl-
• CAS NO: 20428-67-5
• Molecular Formula: C17H19NO2
• Molecular Weight: 269.343
• Mol File: 20428-67-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenepropanamide, b-hydroxy-N,N-dimethyl-b-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanamide, b-hydroxy-N,N-dimethyl-b-phenyl-(20428-67-5)
• EPA Substance Registry System: Benzenepropanamide, b-hydroxy-N,N-dimethyl-b-phenyl-(20428-67-5)

Safety Data

• Hazardous Substances Data: 20428-67-5(Hazardous Substances Data)

Upstream product

• 119-61-9 benzophenone 
• 127-19-5 N,N-dimethyl acetamide 
• 90-90-4 (4-bromophenyl)(phenyl)methanone 

Downstream Products

• 101876-99-7 N,N-dimethyl-3,3-diphenylpropenamide 

Relevant articles and documents

Cerium(III) amide enolate. Addition to aldehydes and ketones

The cerium(III) amide enolates, prepared in situ from the corresponding lithium enolates and anhydrous CeCl3, were found to undergo facile additions to ketones and aldehydes. Yields of the adducts are superior to those obtained using the lithiu

Synthesis of N,N-dimethyl α-aryl and α,α-diarylacetamides by radical nucleophilic substitution reactions

A family of N,N-dimethyl, α-aryl and α,α-diaryl acetamides was synthesized by reaction of aryl halides with N,N-dimethyl acetamide enolate ions in liquid ammonia.The reactions followed the SRN1 mechanism for nucleophilic substitution.They were initiated by light (350 nm), when the aryl halides or aryl halides bearing electron-donating groups were the substrate, and by potassium metal dissolved in liquid ammonia when the substituents on the aryl halides were electron-withdrawing groups. Key Words: SRN1 / nucleophilic substitution / synthesis / acetamide compounds / herbicides