80351-38-8

Basic information

• Product Name: ethyl 1-diphenylmethyl-2-methyl-3-oxo-1,2-diazetidine-4-carboxylate
• Synonyms: ethyl 1-diphenylmethyl-2-methyl-3-oxo-1,2-diazetidine-4-carboxylate
• CAS NO: 80351-38-8
• Molecular Weight: 324.379
• Mol File: 80351-38-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: ethyl 1-diphenylmethyl-2-methyl-3-oxo-1,2-diazetidine-4-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 1-diphenylmethyl-2-methyl-3-oxo-1,2-diazetidine-4-carboxylate(80351-38-8)
• EPA Substance Registry System: ethyl 1-diphenylmethyl-2-methyl-3-oxo-1,2-diazetidine-4-carboxylate(80351-38-8)

Safety Data

• Hazardous Substances Data: 80351-38-8(Hazardous Substances Data)

Upstream product

• 98380-77-9 1-diphenylmethyl-2-methylpyrazolidine-3,5-dione 
• 60295-08-1 tert-butyl 2-(diphenylmethylene)hydrazinecarboxylate 
• 119-61-9 benzophenone 
• 20958-76-3 1-(diphenylmethylene)-3-oxo-1,2-diazetidinium hydroxide, inner salt 
• 79289-53-5 1-benzhydryl-1,2-diazetidin-3-one 
• 541-41-3 chloroformic acid ethyl ester 
• 80351-26-4 1-diphenylmethyl-2-methyl-1,2-diazetidin-3-one 
• 64-17-5 ethanol 
• 98380-81-5 4-diazo-1-diphenylmethyl-2-methylpyrazolidine-3,5-dione 
• 111709-09-2 t-butyl 3-diphenylmethyl-3-ethoxycarbonylacetyl-2-methylcarbazate 
• 111709-08-1 t-butyl 3-diphenylmethyl-2-methylcarbazate 
• 111709-07-0 t-butyl 3-diphenylmethylene-2-methylcarbazate 

Relevant articles and documents

Regioselectivity in the Photochemical Ring Contraction of 4-Diazopyrazolidine-3,5-diones to give Aza-β-lactams

Irradiation of 4-diazopyrazolidine-3,5-diones (15) in the presence of alcohols or water gave mixtures of the isomeric 1,2-diazetidinones (16) and (17), formed by competing photochemical Wolff rearrangement of the two nitrogen groups, followed by reaction of the resulting ketenes with the nucleophile.Some regioselectivity is observed in the ring contraction process, and the relative order of migration of nitrogen groups is NPh>NCHPh2NCH2PhNMe>NCH2CO2Et.The structures of the 1,2-diazetidinones (17c) and (24) were confirmed by X-ray crystallography, and a crystal structure of the diazo compound (15g) was also obtained.Possible reasons for the regioselectivity in the ring contraction are discussed.

Formation of Monocyclic and Bicyclic Aza-β-lactams and Other Novel Heterocycles from 1-(Diphenylmethylene)-3-oxo-1,2-diazetidinium Inner Salt

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