100298-00-8

Basic information

• Product Name: 4-ethyl-1-(3-phenylprop-2-enyl)-2-<((2-trimethylsilyl)ethoxy)carbonyl)methyl>-1,2-diazetidin-3-one
• CAS NO: 100298-00-8
• Molecular Weight: 374.555
• Mol File: 100298-00-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-ethyl-1-(3-phenylprop-2-enyl)-2-<((2-trimethylsilyl)ethoxy)carbonyl)methyl>-1,2-diazetidin-3-one(CAS DataBase Reference)
• NIST Chemistry Reference: 4-ethyl-1-(3-phenylprop-2-enyl)-2-<((2-trimethylsilyl)ethoxy)carbonyl)methyl>-1,2-diazetidin-3-one(100298-00-8)
• EPA Substance Registry System: 4-ethyl-1-(3-phenylprop-2-enyl)-2-<((2-trimethylsilyl)ethoxy)carbonyl)methyl>-1,2-diazetidin-3-one(100298-00-8)

Safety Data

• Hazardous Substances Data: 100298-00-8(Hazardous Substances Data)

Upstream product

• 2916-68-9 2-(Trimethylsilyl)ethanol 
• 100297-89-0 2-(trimethylsilyl)-ethyl chloroacetate 
• 100297-90-3 2-(trimethylsilyl)ethyl iodoacetate 
• 92184-59-3 (1S,4R)-4-Ethyl-1-((E)-3-phenyl-allyl)-[1,2]diazetidin-3-one 

Relevant articles and documents

Synthesis and R eactions of Some 2,2-Disubstitued 1,2-Diazetidin-3-ones: An Intramolecular Aldol Approach to Bicyclic Systems

Several procedures have been developed for alkylation at N-2 of a variety of 1,2-diazetidin-3-ones with N-1 substituent carrying an olefinic bond.Ozonolysis yielded aldehydes which were subjected to aldol cyclization conditions.The products proved to be rearranged bicyclic products arising from intramolecular ring opening of the 1,2-diazetidin-3-one lactam bond by the secondary hydroxyl group formed in the aldol reaction.