119493-02-6

Basic information

• Product Name: N-Benzyl-2-phenoxy-malonamic acid methyl ester
• Synonyms: N-Benzyl-2-phenoxy-malonamic acid methyl ester
• CAS NO: 119493-02-6
• Molecular Weight: 299.326
• Mol File: 119493-02-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-Benzyl-2-phenoxy-malonamic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: N-Benzyl-2-phenoxy-malonamic acid methyl ester(119493-02-6)
• EPA Substance Registry System: N-Benzyl-2-phenoxy-malonamic acid methyl ester(119493-02-6)

Safety Data

• Hazardous Substances Data: 119493-02-6(Hazardous Substances Data)

Upstream product

• 119492-92-1 1-benzyl-4,4-bis-methylsulfanyl-3-phenoxyazetidin-2-one 
• 100-46-9 benzylamine 
• 701-99-5 Phenoxyacetyl chloride 
• 119492-95-4 1-Benzyl-3-phenoxy-5,8-dithia-1-aza-spiro[3.4]octan-2-one 
• 54985-63-6 N-(Benzyl)imidodithiokohlensaeure-S,S'-dimethylester 
• 2080-48-0 N-Benzyl-1,3-dithiolane-2-imine 

Relevant articles and documents

Synthesis of 4-Unsubstituted β-Lactams via Dithiocarbonimidates

Cycloaddition of dithiocarbonimidate 1 to the ketene generated in situ from phenoxyacetylchloride in the presence of triethylamine affords the 4-dithioalkyl-2-azetidinones 2 in good yields.Facile conversion of 2 to the 4-unsubstituted β-lactams 3 can be accomplished by desulfurization with Raney-Nickel.Formation of several interesting products during attempts to bring a carbonyl function at C-4 in 2 has also been described.