1284574-36-2

Basic information

• Product Name: N-benzyl-2-(3,4-dimethoxyphenyl)-2-oxoacetamide
• Synonyms: N-benzyl-2-(3,4-dimethoxyphenyl)-2-oxoacetamide
• CAS NO: 1284574-36-2
• Molecular Weight: 299.326
• Mol File: 1284574-36-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-benzyl-2-(3,4-dimethoxyphenyl)-2-oxoacetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-2-(3,4-dimethoxyphenyl)-2-oxoacetamide(1284574-36-2)
• EPA Substance Registry System: N-benzyl-2-(3,4-dimethoxyphenyl)-2-oxoacetamide(1284574-36-2)

Safety Data

• Hazardous Substances Data: 1284574-36-2(Hazardous Substances Data)

Upstream product

• 127901-46-6 N-methyl-3,4-dimethoxyphenylglyoxamide 
• 100-46-9 benzylamine 
• 4732-70-1 3,4-dimethoxyphenylglyoxylic acid 
• 5460-32-2 1-iodo-3,4-dimethoxybenzene 
• 82102-37-2 9-methyl-9H-fluorene-9-carbonyl chloride 

Downstream Products

• 1386820-20-7 C₁₇H₁₉NO₄ 
• 101582-87-0 N-benzyl-1-(3',4'-dimethoxyphenyl)-2-aminoethanol 

Relevant articles and documents

Diversification of α-ketoamides: Via transamidation reactions with alkyl and benzyl amines at room temperature

A wide range of N-tosyl α-ketoamides underwent transamidation with various alkyl amines in the absence of a catalyst, base, or additive. On the other hand, transamidation in N-Boc α-ketoamides was achieved in the presence of Cs2CO3. The reactions proceede

Palladium-catalyzed double carbonylation using near stoichiometric carbon monoxide: Expedient access to substituted 13C2-labeled phenethylamines

A novel and general approach for 13C2- and 2H-labeled phenethylamine derivatives has been developed, based on a highly convergent single-step assembly of the carbon skeleton. The efficient incorporation of two carbon-13 isotopes into phenethylamines was accomplished using a palladium-catalyzed double carbonylation of aryl iodides with near stoichiometric carbon monoxide.