917110-35-1

Basic information

• Product Name: (3S,4S)-3-Bromo-3-((2S,3R)-3-ethyl-oxiranyl)-4-phenyl-1-((S)-1-phenyl-ethyl)-azetidin-2-one
• Synonyms: (3S,4S)-3-Bromo-3-((2S,3R)-3-ethyl-oxiranyl)-4-phenyl-1-((S)-1-phenyl-ethyl)-azetidin-2-one
• CAS NO: 917110-35-1
• Molecular Weight: 400.315
• Mol File: 917110-35-1.mol

Chemical Properties

• CAS DataBase Reference: (3S,4S)-3-Bromo-3-((2S,3R)-3-ethyl-oxiranyl)-4-phenyl-1-((S)-1-phenyl-ethyl)-azetidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (3S,4S)-3-Bromo-3-((2S,3R)-3-ethyl-oxiranyl)-4-phenyl-1-((S)-1-phenyl-ethyl)-azetidin-2-one(917110-35-1)
• EPA Substance Registry System: (3S,4S)-3-Bromo-3-((2S,3R)-3-ethyl-oxiranyl)-4-phenyl-1-((S)-1-phenyl-ethyl)-azetidin-2-one(917110-35-1)

Safety Data

• Hazardous Substances Data: 917110-35-1(Hazardous Substances Data)

Upstream product

• 847548-22-5 (1S',3R,4S)-3-bromo-3-but-1-enyl-4-phenyl-1-(1-phenylethyl)azetidin-2-one 

Downstream Products

• 917110-47-5 (2S,3R,6S)-2-((S)-1-Azido-propyl)-6-phenyl-5-((S)-1-phenyl-ethyl)-1-oxa-5-aza-spiro[2.3]hexan-4-one 
• 917110-41-9 (3S,4S)-3-((1S,2S)-2-Azido-1-hydroxy-butyl)-3-bromo-4-phenyl-1-((S)-1-phenyl-ethyl)-azetidin-2-one 

Relevant articles and documents

A microwave-enhanced, lewis acid-catalyzed synthesis of 1,3-dioxolanes and oxazolines from epoxides

A fast and highly regio- and stereoselective transformation of non-conventional β-lactam- b containing epoxides into the corresponding cyclic 1,3-dioxolanes and oxazolines is herein reported, using microwave irradiation as an efficient source of energy, in the presence of stoichiometric or catalytic amounts of Lewis acids, without an additional solvent. These cyclic compounds are the protected forms of diols and amino alcohols.

Synthesis and biological evaluation of azido- and aziridino-hydroxyl- β-lactams through stereo- and regioselective epoxide ring opening

(Chemical Equation Presented) Two new classes of azido- and aziridino-hydroxyl-β-lactam containing structures have been prepared by means of a stereo- and regioselective epoxide ring opening. The straightforwardness of the procedure makes this strategy us