122673-11-4

Basic information

• Product Name: 1-(4-methoxyphenyl)-4-(α-methylstyryl)azetidin-2-one
• Synonyms: 1-(4-methoxyphenyl)-4-(α-methylstyryl)azetidin-2-one
• CAS NO: 122673-11-4
• Molecular Weight: 293.365
• Mol File: 122673-11-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(4-methoxyphenyl)-4-(α-methylstyryl)azetidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-methoxyphenyl)-4-(α-methylstyryl)azetidin-2-one(122673-11-4)
• EPA Substance Registry System: 1-(4-methoxyphenyl)-4-(α-methylstyryl)azetidin-2-one(122673-11-4)

Safety Data

• Hazardous Substances Data: 122673-11-4(Hazardous Substances Data)

Upstream product

• 108908-63-0 N-4-methoxyphenyl-α-methylcinnamylideneamine 
• 105-36-2 ethyl bromoacetate 
• 100239-15-4 (E)-4-methoxy-N-((E)-2-methyl-3-phenylallylidene)aniline 

Downstream Products

• 122598-60-1 trans-3-(1-acetoxyethyl)-1-(4-methoxyphenyl)-4-(α-methylstyryl)azetidin-2-one 
• 123003-90-7 trans-4-acetoxy-3-(1-acetoxyethyl)-1-(4-methoxyphenyl)azetidin-2-one 
• 123003-89-4 trans-3-(1-acetoxyethyl)-4-acetyl-1-(4-methoxyphenyl)azetidin-2-one 
• 123003-79-2 trans-4-acetoxy-3-isopropyl-1-(4-methoxyphenyl)azetidin-2-one 
• 119067-41-3 trans-4-acetoxy-3-ethyl-1-(4-methoxyphenyl)azetidin-2-one 
• 123003-78-1 trans-4-acetyl-3-isopropyl-1-(4-methoxyphenyl)azetidin-2-one 
• 127756-72-3 4-acetoxy-1-(4-methoxyphenyl)azetidin-2-one 
• 118991-44-9 4-Acetyl-1-(4-methoxy-phenyl)-azetidin-2-one 
• 100239-22-3 trans-3-(1-hydroxyethyl)-4-(α-methylstyryl)-1-(4-methoxyphenyl)azetidin-2-one 
• 122598-57-6 trans-3-isopropyl-4-(α-methylstyryl)-1-(4-methoxyphenyl)azetidin-2-one 
• 118991-38-1 trans-3-ethyl-4-(α-methylstyryl)-1-(4-methoxyphenyl)azetidin-2-one 
• 118991-40-5 trans-4-acetyl-3-ethyl-1-(4-methoxyphenyl)azetidin-2-one 
• 123003-88-3 trans-3-acetyl-4-(α-methylstyryl)-1-(4-methoxyphenyl)azetidin-2-one 

Relevant articles and documents

The α-Bromoester-Imine Condensation promoted by Zinc-Trimethylchlorosilane: A Stereospecific Short Formal Synthesis of (+/-)-Carbapenem Antibiotics and Realated Compounds

Ethyl bromoacetate reacts with imines in the presence of zinc activated by trimethylchlorosilane to give high yields of 3-unsubstituted β-lactams.

A short formal synthesis of the carbapenem antibiotic (±)-PS-5

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