592532-30-4

Basic information

• Product Name: Pentaneperoxoic acid, 5-oxo-5-(phenylmethoxy)-4-[[(phenylmethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester, (4S)-
• CAS NO: 592532-30-4
• Molecular Formula: C24H29NO7
• Molecular Weight: 443.497
• Mol File: 592532-30-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Pentaneperoxoic acid, 5-oxo-5-(phenylmethoxy)-4-[[(phenylmethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester, (4S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Pentaneperoxoic acid, 5-oxo-5-(phenylmethoxy)-4-[[(phenylmethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester, (4S)-(592532-30-4)
• EPA Substance Registry System: Pentaneperoxoic acid, 5-oxo-5-(phenylmethoxy)-4-[[(phenylmethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester, (4S)-(592532-30-4)

Safety Data

• Hazardous Substances Data: 592532-30-4(Hazardous Substances Data)

Upstream product

• 75-91-2 tert.-butylhydroperoxide 
• 65706-99-2 1-benzyl N-carbobenzoxy-L-glutamate 

Relevant articles and documents

Retention of configuration in photolytic decarboxylation of peresters to form chiral acetals and ethers

(Chemical Equation Presented) Peresters generate ethers in good yields when photolyzed in the absence of solvent using short wavelength UV light. At -78 °C or below, the process proceeds predominantly with retention of configuration at the site adjacent to the carbonyl where the decarboxylation occurs, but increase in temperature results in loss of stereochemical control. Chiral acyclic acetals can be prepared using precursors derived from tartaric or malic acids.