22628-31-5

Basic information

• Product Name: syn-3-methyl-1,4-diphenylazetidin-2-one
• Synonyms: syn-3-methyl-1,4-diphenylazetidin-2-one
• CAS NO: 22628-31-5
• Molecular Weight: 237.301
• Mol File: 22628-31-5.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: syn-3-methyl-1,4-diphenylazetidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: syn-3-methyl-1,4-diphenylazetidin-2-one(22628-31-5)
• EPA Substance Registry System: syn-3-methyl-1,4-diphenylazetidin-2-one(22628-31-5)

Safety Data

• Hazardous Substances Data: 22628-31-5(Hazardous Substances Data)

Upstream product

• 538-51-2 benzylidene phenylamine 
• 105-37-3 Ethyl propionate 
• 37612-61-6 1-(3,5-dimethyl-1H-pyrazol-1-yl)propan-1-one 
• 37612-62-7 1-butyryl-3,5-dimethyl-1H-pyrazole 
• 1750-36-3 (E)-N-benzylidenebenzenamine 
• 535-11-5 Ethyl 2-bromopropionate 
• 76943-94-7 (Z)-1-(tert-butylthio)-1-trimethylsilyloxyprop-1-ene 
• 62-53-3 aniline 
• 63584-42-9 (Z)-1-ethylthio-1-(trimethylsiloxy)propene 
• 63584-42-9 {[(1E)-1-(ethylthio)prop-1-enyl]oxy}(trimethyl)silane 
• 24948-35-4 2-Methyl-3-phenyl-3-phenylamino-propionic acid 
• 34880-70-1 [1-methoxyprop-1-enyloxy]trimethylsilane 
• 292638-85-8 acrylic acid methyl ester 
• 100-52-7 benzaldehyde 

Downstream Products

• 24948-31-0 syn-methyl 2-methyl-3-phenyl-3-(phenylamino)propanoate 
• 24948-35-4 (2RS:3RS)-3-anilino-2-methyl-3-phenyl-propionic acid 

Relevant articles and documents

Highly trans-selective synthesis of β-lactams by tandem phenoxide anion-catalyzed Mannich-type addition and cyclization

Highly trans-selective synthesis of β-lactams by tandem Lewis base-catalyzed Mannich-type addition and cyclization was established; that is, reaction of benzylideneanilines and trimethylsilyl enolates derived from S-ethyl thioates proceeded smoothly to af

Stereodefined homopropargyl amines by tandem nucleophilic addition/fragmentation of dihydropyridone triflates

Dihydropyridone (DHPD) triflates undergo nucleophile-triggered fragmentation to provide homopropargyl amine derivatives, the stereochemistry of which is defined by starting from readily available β-amino esters.

The synthesis of β-lactams via a one-pot Reformatsky reaction of imines promoted by Zn/Cp2TiCl2 (cat.)

In the presence of Zn/Cp2TiCl2 (cat.) α-bromoacetates, γ-bromocrotonates or α-bromomethylacrylates react with imines in one-pot to form β-lactams, 3-vinyl-β-lactams or α-methylene-γ-lactams, respectively, at room temperature without