214412-66-5

Basic information

• Product Name: (1S,5R)-6-Benzyloxycarbonylmethoxy-7-oxo-2,6-diaza-bicyclo[3.2.0]heptane-2-carboxylic acid tert-butyl ester
• Synonyms: (1S,5R)-6-Benzyloxycarbonylmethoxy-7-oxo-2,6-diaza-bicyclo[3.2.0]heptane-2-carboxylic acid tert-butyl ester
• CAS NO: 214412-66-5
• Molecular Weight: 376.409
• Mol File: 214412-66-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,5R)-6-Benzyloxycarbonylmethoxy-7-oxo-2,6-diaza-bicyclo[3.2.0]heptane-2-carboxylic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,5R)-6-Benzyloxycarbonylmethoxy-7-oxo-2,6-diaza-bicyclo[3.2.0]heptane-2-carboxylic acid tert-butyl ester(214412-66-5)
• EPA Substance Registry System: (1S,5R)-6-Benzyloxycarbonylmethoxy-7-oxo-2,6-diaza-bicyclo[3.2.0]heptane-2-carboxylic acid tert-butyl ester(214412-66-5)

Safety Data

• Hazardous Substances Data: 214412-66-5(Hazardous Substances Data)

Upstream product

• 214412-65-4 (1R,5R)-6-hydroxy-7-oxo-2,6-diazabicyclo[3.2.0]heptane-2-carboxylic acid tert-butyl ester 
• 5437-45-6 Benzyl bromoacetate 
• 214412-60-9 [(1S,2S)-1-Benzyloxycarbamoyl-2-hydroxy-4-(tetrahydro-pyran-2-yloxy)-butyl]-carbamic acid tert-butyl ester 
• 214412-64-3 Methanesulfonic acid 2-((2R,3S)-1-benzyloxy-3-tert-butoxycarbonylamino-4-oxo-azetidin-2-yl)-ethyl ester 
• 214412-61-0 {(3S,4R)-1-Benzyloxy-2-oxo-4-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-azetidin-3-yl}-carbamic acid tert-butyl ester 
• 214412-59-6 (1S,2S)-1-carboxy-2-hydroxy-4-((R,S)-tetrahydropyran-2-yloxy)butylcarbamic acid tert-butyl ester 
• 214412-57-4 (2R,3S)-3-[2-((R,S)-tetrahydropyran-2-yloxy)ethyl]oxiran-2-ylmethanol 
• 187039-59-4 (1S,5R)-6-Benzyloxy-7-oxo-2,6-diaza-bicyclo[3.2.0]heptane-2-carboxylic acid tert-butyl ester 
• 92844-99-0 (2E)-5-<(2-tetrahydropyranyl)oxy>pent-2-en-1-ol 
• 51442-80-9 5-(tetrahydro-2H-pyran-2-yloxy)-2-pentyn-1-ol 
• 214412-63-2 [(2R,3S)-1-Benzyloxy-2-(2-hydroxy-ethyl)-4-oxo-azetidin-3-yl]-carbamic acid tert-butyl ester 
• 214412-58-5 (2R,3S)-3-[2-((R,S)-tetrahydropyran-2-yloxy)ethyl]oxiran-2-carboxylic acid 

Relevant articles and documents

Structure-based design of β-lactamase inhibitors. 2. Synthesis and evaluation of bridged sulfactams and oxamazins

A series of bridged monocyclic β-lactams activated by various groups on the β-lactam nitrogen (X = OCH2CO2H, OSO3H) has been synthesized and evaluated. Among them, the bridged sulfactams (X = OSO3H) were found t