87568-43-2

Basic information

• Product Name: 2,3-Azetidinedione, 1-(4-methoxyphenyl)-
• CAS NO: 87568-43-2
• Molecular Formula: C10H9NO3
• Molecular Weight: 191.186
• Mol File: 87568-43-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,3-Azetidinedione, 1-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-Azetidinedione, 1-(4-methoxyphenyl)-(87568-43-2)
• EPA Substance Registry System: 2,3-Azetidinedione, 1-(4-methoxyphenyl)-(87568-43-2)

Safety Data

• Hazardous Substances Data: 87568-43-2(Hazardous Substances Data)

Upstream product

• 69193-56-2 1-(4-methoxyphenyl)-3-methylideneazetidin-2-one 
• 20109-30-2 6,6'-dimethyl-2,2'-sulfanediyl-di-phenol 
• 87568-42-1 1-(p-methoxyphenyl)-3-methyl-3-(phenylsulfinyl)azetidin-2-one 
• 87568-30-7 1-(p-methoxyphenyl)-3-methyl-3-(phenylthio)azetidin-2-one 
• 7274-71-7 N-(4-methoxyphenyl)-2-methylacrylamide 
• 228720-78-3 1-(4'-methoxyphenyl)-3-acetoxy-4,4-bis(ethylthio)azetidin-2-one 
• 228720-63-6 1-(4'-methoxy-phenyl)-3-acetoxy-4,4-bis(methylthio)azetidin-2-one 
• 228720-64-7 1-(4'-methoxyphenyl)-3-acetoxy-azetidin-2-one 
• 142389-21-7 C₁₂H₁₇NOS₂ 
• 33692-63-6 dimethyl N-(para-methoxyphenyl)-dithio-carbonimidate 
• 228720-65-8 (+/-)-1-(4'-methoxyphenyl)-3-hydroxy-azetidin-2-one 

Downstream Products

• 87568-46-5 3-(((benzyloxy)carbonyl)amino)-1-(p-methoxyphenyl)azetidin-2-one 
• 87568-45-4 3-amino-1-(p-methoxyphenyl)azetidin-2-one 
• 87568-44-3 1-(p-methoxyphenyl)azetidin-2-one 3-oxime 

Relevant articles and documents

Chemo-enzymatic synthesis of chiral 3-hydroxy-azetidin-2-ones

n-Tributyltin hydride reduction of 3-acetoxy-4,4-bis(alkylthio)- azetidin-2-ones 4a and 4b produces 4-unsubstituted azetidinone 5 and 4- alkylthio-azetidin-2-one 9 respectively. Azetidin-2,3-diones 8,11,13 which can be conveniently prepared by basic hydro

Synthesis of β-lactam antibiotics by the sulfeno-cycloamination

A novel efficient beta -lactam synthesis was achieved by two successive processes (sulfeno-cycloamination), addition of phenysulfenyl chloride to alpha , beta -unsaturated amides followed by base treatment. Key synthetic intermediates of monobactams and nocardicin derivatives were obtained via this method. construction of the 1-carbapenam ring system by the sulfenocycloamination is also described.