606144-84-7

Basic information

• Product Name: methyl (3S,4R)-4-({(2R)-2-[(tert-butoxycarbonyl)amino]-2-phenylethyl}oxy)-4-phenyl-3-(phenylseleno)butanoate
• Synonyms: methyl (3S,4R)-4-({(2R)-2-[(tert-butoxycarbonyl)amino]-2-phenylethyl}oxy)-4-phenyl-3-(phenylseleno)butanoate
• CAS NO: 606144-84-7
• Molecular Weight: 568.572
• Mol File: 606144-84-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl (3S,4R)-4-({(2R)-2-[(tert-butoxycarbonyl)amino]-2-phenylethyl}oxy)-4-phenyl-3-(phenylseleno)butanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (3S,4R)-4-({(2R)-2-[(tert-butoxycarbonyl)amino]-2-phenylethyl}oxy)-4-phenyl-3-(phenylseleno)butanoate(606144-84-7)
• EPA Substance Registry System: methyl (3S,4R)-4-({(2R)-2-[(tert-butoxycarbonyl)amino]-2-phenylethyl}oxy)-4-phenyl-3-(phenylseleno)butanoate(606144-84-7)

Safety Data

• Hazardous Substances Data: 606144-84-7(Hazardous Substances Data)

Upstream product

• 71098-88-9 N-phenylselanylphthalimide 
• 91083-82-8 (E)-methyl 4-phenylbut-3-enoate 
• 67341-01-9 (R)-N-(tert-butoxycarbonyl)phenylglycinol 
• 24424-99-5 di-tert-butyl dicarbonate 

Relevant articles and documents

Selenium-promoted synthesis of enantiomerically pure substituted morpholines starting from alkenes and chiral aminoalcohols

Enantiomerically pure 2,3,5-trisubstituted morpholines with two newly created stereocenters have been prepared by a short synthetic sequence having as the key step the selenium-promoted addition of (R)-phenylglycinol to a substituted alkene.