27983-93-3

Basic information

• Product Name: 3,3-dimethyl-N-phenyl-2-azetidinone
• Synonyms: 3,3-dimethyl-N-phenyl-2-azetidinone
• CAS NO: 27983-93-3
• Molecular Weight: 175.23
• Mol File: 27983-93-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3,3-dimethyl-N-phenyl-2-azetidinone(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3-dimethyl-N-phenyl-2-azetidinone(27983-93-3)
• EPA Substance Registry System: 3,3-dimethyl-N-phenyl-2-azetidinone(27983-93-3)

Safety Data

• Hazardous Substances Data: 27983-93-3(Hazardous Substances Data)

Upstream product

• 13511-38-1 3-chloropivalic acid 
• 115363-85-4 3-tert-Butylsulfanyl-2,2-dimethyl-propionyl chloride 
• 99314-07-5 4-<(1,1-dimethylethyl)thio>-3,3-dimethyl-N-(o-iodophenyl)-2-azetidinone 
• 99314-09-7 N-(o-bromophenyl)-4-<(1,1-dimethylethyl)thio>-3,3-dimethyl-2-azetidinone 
• 115363-90-1 3-tert-Butylsulfanyl-3-chloro-2,2-dimethyl-propionyl chloride 
• 615-43-0 2-iodophenylamine 
• 62-53-3 aniline 
• 4300-97-4 3-Chloropivaloyl chloride 
• 3009-97-0 N-phenylglycinonitrile 
• 97-62-1 Ethyl isobutyrate 
• 82820-74-4 N-phenyl β-chloro-α,α-dimethylpropionamide 
• 99314-08-6 3,3-dimethyl-4-mercapto-N-phenyl-2-azetidinone 

Downstream Products

• 115437-14-4 4-(phenylamino)-3,3-dimethyl-2-butanone 
• 22745-26-2 3,3-Dimethyl-1-phenylazetidin 
• 115437-08-6 2-methylene-3,3-dimethyl-1-phenylazetidine 
• 103-71-9 phenyl isocyanate 
• 115-11-7 isobutene 
• 96594-26-2 3,3-Dimethyl-1-phenyl-2-azetidinthion 
• 82820-74-4 N-phenyl β-chloro-α,α-dimethylpropionamide 
• 106576-12-9 Benzoic acid 3,3-dimethyl-4-oxo-1-phenyl-azetidin-2-yl ester 

Relevant articles and documents

New synthesis of 2-methyleneaziridines and 2-methyleneazetidines by dimethyl titanocene mediated methylenation of α- and β-lactams

2-Methyleneaziridines and 2-methyleneazetidines were synthesized via a titanium mediated olefination procedure starting from the corresponding α- lactams and β-lactams. (C) 2000 Elsevier Science Ltd.

A Convenient Synthesis of 4-Unsubstituted β-Lactams

The reaction of lithium ester enolates with N-(cyanomethyl)amines affords 4-unsubstituted β-lactams in good yields, see eq 1.The N-1 substituent can be varied widely, as can the C-3 substituents, which can be H, alkyl, SPh, NH2, or NHCOR.The preparation o

A one-pot synthesis of β-lactams by the reaction of β-haloacyl chlorides with α-amino acids

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