858884-54-5

Basic information

• Product Name: (R)-{(2R,3R)-3-[((R)-Benzyloxycarbonyl-phenyl-methyl)-carbamoyl]-2,3-dihydroxy-propionylamino}-phenyl-acetic acid benzyl ester
• Synonyms: (R)-{(2R,3R)-3-[((R)-Benzyloxycarbonyl-phenyl-methyl)-carbamoyl]-2,3-dihydroxy-propionylamino}-phenyl-acetic acid benzyl ester
• CAS NO: 858884-54-5
• Molecular Weight: 596.637
• Mol File: 858884-54-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-{(2R,3R)-3-[((R)-Benzyloxycarbonyl-phenyl-methyl)-carbamoyl]-2,3-dihydroxy-propionylamino}-phenyl-acetic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-{(2R,3R)-3-[((R)-Benzyloxycarbonyl-phenyl-methyl)-carbamoyl]-2,3-dihydroxy-propionylamino}-phenyl-acetic acid benzyl ester(858884-54-5)
• EPA Substance Registry System: (R)-{(2R,3R)-3-[((R)-Benzyloxycarbonyl-phenyl-methyl)-carbamoyl]-2,3-dihydroxy-propionylamino}-phenyl-acetic acid benzyl ester(858884-54-5)

Safety Data

• Hazardous Substances Data: 858884-54-5(Hazardous Substances Data)

Upstream product

• 87-69-4 L-Tartaric acid 
• 133545-89-8 [(1R)-2-(benzyloxy)-2-oxo-1-phenylethyl]ammonium 4-methyl-1-benzensulfonate 
• 100-51-6 benzyl alcohol 
• 104-15-4 toluene-4-sulfonic acid 
• 875-74-1 (R)-phenylglycine 

Relevant articles and documents

Synthesis of a library of chiral α-amino acid-based borate counteranions and their application to copper catalyzed olefin cyclopropanation

Twenty borate counteranions have been prepared from tartaric acid and α-amino acid derivatives. Ion pairing of these anions to a copper cation can be used to induce enantioselectivity into the copper catalyzed cyclopropanation of styrene. Structural modification of the anion provides insight into the importance of each component of the counteranion in asymmetric induction.