342406-53-5

Basic information

• Product Name: N¹-benzyl-N²-phenyloxalamide
• Synonyms: N¹-benzyl-N²-phenyloxalamide
• CAS NO: 342406-53-5
• Molecular Weight: 254.288
• Mol File: 342406-53-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N¹-benzyl-N²-phenyloxalamide(CAS DataBase Reference)
• NIST Chemistry Reference: N¹-benzyl-N²-phenyloxalamide(342406-53-5)
• EPA Substance Registry System: N¹-benzyl-N²-phenyloxalamide(342406-53-5)

Safety Data

• Hazardous Substances Data: 342406-53-5(Hazardous Substances Data)

Upstream product

• 100-46-9 benzylamine 
• 959-66-0 3-oxo-3-phenylpropionanilide 
• 7142-72-5 N-benzyloxamic acid ethyl ester 
• 62-53-3 aniline 
• 1457-85-8 Ethyl oxanilate 
• 859068-71-6 benzyl-aminooxalyl azide 
• 71290-28-3 N-benzyl-2-hydrazinyl-2-oxoacetamide 

Downstream Products

• 64469-50-7 1-benzyl-3-phenyl-imidazolidine 
• 58077-34-2 N¹-benzyl-N²-phenylethane-1,2-diamine 
• 10197-25-8 N-Benzyl-N'-phenyl-dithiooxalamide 

Relevant articles and documents

Selective amidation by a photocatalyzed umpolung reaction

A metal-catalyzed organic transformation merged with another organophotocatalyst has been developed under mild conditions for production of α-ketoamides. CuI-catalyzed highly selective and rapid COCH2-amidation in the presence of electrophilic CαO bonds, which is synchronized by an eosin Y (EY)-photocatalyst, furnishes a wide range of labile α-ketoamides, unsymmetrical oxalamides and chiral analogues on the treatment of 1,3-dicarbonyls with amines, PhIO and LED light at room temperature. The current strategy opens up a new avenue to making photocatalysis a common synthetic tool for large-scale production in academia and industry.