1334521-76-4

Basic information

• Product Name: benzyl 2-(((1R,5R)-2-benzoyl-3,3-dimethyl-7-oxo-4-thia-2,6-diazabicyclo[3.2.0]heptan-6-yl)oxy)acetate
• Synonyms: benzyl 2-(((1R,5R)-2-benzoyl-3,3-dimethyl-7-oxo-4-thia-2,6-diazabicyclo[3.2.0]heptan-6-yl)oxy)acetate
• CAS NO: 1334521-76-4
• Molecular Weight: 426.493
• Mol File: 1334521-76-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: benzyl 2-(((1R,5R)-2-benzoyl-3,3-dimethyl-7-oxo-4-thia-2,6-diazabicyclo[3.2.0]heptan-6-yl)oxy)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 2-(((1R,5R)-2-benzoyl-3,3-dimethyl-7-oxo-4-thia-2,6-diazabicyclo[3.2.0]heptan-6-yl)oxy)acetate(1334521-76-4)
• EPA Substance Registry System: benzyl 2-(((1R,5R)-2-benzoyl-3,3-dimethyl-7-oxo-4-thia-2,6-diazabicyclo[3.2.0]heptan-6-yl)oxy)acetate(1334521-76-4)

Safety Data

• Hazardous Substances Data: 1334521-76-4(Hazardous Substances Data)

Upstream product

• 57704-00-4 3-benzoyl-2,2-dimethylthiazolidine-4R-carboxylic acid 
• 46230-31-3 benzyl 2-(aminooxy)acetate 
• 1334521-62-8 benzyl 2-(((4R,5S)-3-benzoyl-5-hydroxy-2,2-dimethylthiazolidine-4-carboxamido)oxy)acetate 
• 1334521-50-4 (R)-benzyl 2-((3-benzoyl-2,2-dimethylthiazolidine-4-carboxamido)oxy)acetate 

Relevant articles and documents

Asymmetric synthesis of monocyclic β-lactams from l-cysteine using photochemistry

An asymmetric method to synthesize cis-configured β-lactams using photochemistry has been developed. Aerobic photo-oxidation of l-cysteine-derived thiazolidine hydroxamate esters afforded C-3 hydroxylated products which when cyclized and deprotected gave