438566-45-1

Basic information

• Product Name: (3R,4S)-3-benzyloxy-1-[(2S)-2-(1-ethyl-1-methoxypropyl)pyrrolidin-1-yl]-4-phenylazetidin-2-one
• Synonyms: (3R,4S)-3-benzyloxy-1-[(2S)-2-(1-ethyl-1-methoxypropyl)pyrrolidin-1-yl]-4-phenylazetidin-2-one
• CAS NO: 438566-45-1
• Molecular Weight: 422.568
• Mol File: 438566-45-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3R,4S)-3-benzyloxy-1-[(2S)-2-(1-ethyl-1-methoxypropyl)pyrrolidin-1-yl]-4-phenylazetidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (3R,4S)-3-benzyloxy-1-[(2S)-2-(1-ethyl-1-methoxypropyl)pyrrolidin-1-yl]-4-phenylazetidin-2-one(438566-45-1)
• EPA Substance Registry System: (3R,4S)-3-benzyloxy-1-[(2S)-2-(1-ethyl-1-methoxypropyl)pyrrolidin-1-yl]-4-phenylazetidin-2-one(438566-45-1)

Safety Data

• Hazardous Substances Data: 438566-45-1(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 118535-62-9 (S)-(-)-1-amino-2-(1'-methoxy-1'-ethylpropyl)pyrrolidine 
• 19810-31-2 Benzyloxyacetyl chloride 

Downstream Products

• 136561-53-0 (2R,3S)-2-hydroxy-3-amino-3-phenylpropionic acid 
• 132127-34-5 (3R,4S)-3-hydroxy-4-phenylazetidin-2-one 
• 130632-19-8 (-)-(3R,4S)-3-Benzyloxy-4-phenylazetidin-2-one 

Relevant articles and documents

Studies on stereoselective [2+2] cycloadditions between N,N-dialkylhydrazones and ketenes

Staudinger-like cycloadditions between chiral, non-racemic N,N-dialkylhydrazones 1 and functionalized ketenes constitute an efficient methodology for the stereoselective construction of the β-lactam ring. The potential for fine tuning of the dialkylamino