146467-05-2

Basic information

• Product Name: 1-benzyl-3S-benzyloxy-4R-[1'R,2'S-O-isopropylidene-3-oxo]propyl-azetidin-2-one
• Synonyms: 1-benzyl-3S-benzyloxy-4R-[1'R,2'S-O-isopropylidene-3-oxo]propyl-azetidin-2-one
• CAS NO: 146467-05-2
• Molecular Weight: 395.455
• Mol File: 146467-05-2.mol

Chemical Properties

• CAS DataBase Reference: 1-benzyl-3S-benzyloxy-4R-[1'R,2'S-O-isopropylidene-3-oxo]propyl-azetidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-benzyl-3S-benzyloxy-4R-[1'R,2'S-O-isopropylidene-3-oxo]propyl-azetidin-2-one(146467-05-2)
• EPA Substance Registry System: 1-benzyl-3S-benzyloxy-4R-[1'R,2'S-O-isopropylidene-3-oxo]propyl-azetidin-2-one(146467-05-2)

Safety Data

• Hazardous Substances Data: 146467-05-2(Hazardous Substances Data)

Upstream product

• 146467-03-0 cis-1-benzyl-3S-benzyloxy-4R-[1'R,2'S,3'R,4'-di-O-isopropylidene]butyl-azetidin-2-one 
• 146467-04-1 1-benzyl-3S-benzyloxy-4R-[1'R,2'S-O-isopropylidene-3'R,4'-dihydroxy]butyl azetidin-2-one 

Downstream Products

• 146467-07-4 1-benzyl-3S-hydroxy-4R-[1'R,2'R-O-isopropylidene-3'-hydroxy]propyl-azetidin-2-one 
• 146467-10-9 (2S,3S)-3-Amino-3-((4R,5R)-2,2-dimethyl-5-trityloxymethyl-[1,3]dioxolan-4-yl)-propane-1,2-diol 
• 146467-09-6 (2R,3R-O-isopropylidene)-4S-(N-benzylamino)-5R,6-dihydroxyhexyl-triphenylmethyl ether 
• 146467-08-5 1-benzyl-3S-hydroxy-4R-[1'R,2'R-O-isopropylidene-3'-triphenylmethoxy]propyl-azetidin-2-one 
• 146467-11-0 [(1S,2S)-1-((4R,5R)-2,2-Dimethyl-5-trityloxymethyl-[1,3]dioxolan-4-yl)-2,3-dihydroxy-propyl]-carbamic acid tert-butyl ester 
• 146467-12-1 (R)-tert-Butoxycarbonylamino-((4R,5R)-2,2-dimethyl-5-trityloxymethyl-[1,3]dioxolan-4-yl)-acetic acid 
• 1169757-48-5 C₃₆H₅₁NO₄ 
• 146467-06-3 1-benzyl-3S-benzyloxy-4R-[1'R,2'R-O-isopropylidene-3'-hydroxy]propyl-azetidin-2-one 

Relevant articles and documents

Polyhydroxy amino acid derivatives via β-lactams using enantiospecific approaches and microwave techniques

Enantiospecific synthesis has been developed for α-hydroxy β-lactams of predictable absolute configuration starting with readily available carbohydrates. Stereospecific approaches and microwave assisted chemical reactions have been utilized for the prepar

Versatile β-Lactam Synthons: Enantiospecific Synthesis of (-)-Polyoxamic Acid

An optically pure cis-α-hydroxy β-lactam of predictable absolute configuration prepared from readily available D-mannitol has been utilized for the synthesis of the non-natural enantiomer of polyoxamic acid through a series of stereospecific reactions.