511546-47-7

Basic information

• Product Name: C₆₀H₇₉N₉O₂₈
• Synonyms: C₆₀H₇₉N₉O₂₈
• CAS NO: 511546-47-7
• Molecular Weight: 1374.33
• Mol File: 511546-47-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₆₀H₇₉N₉O₂₈(CAS DataBase Reference)
• NIST Chemistry Reference: C₆₀H₇₉N₉O₂₈(511546-47-7)
• EPA Substance Registry System: C₆₀H₇₉N₉O₂₈(511546-47-7)

Safety Data

• Hazardous Substances Data: 511546-47-7(Hazardous Substances Data)

Upstream product

• 511546-44-4 C₄₆H₆₂N₆O₂₄ 
• 118409-71-5 {2-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(4-hydroxy-phenyl)-propionylamino]-acetylamino}-acetic acid 
• 21778-69-8 tyrosylglycylglycine 
• 191591-11-4 L-tyrosylglycylglycine methyl ester 

Relevant articles and documents

Efficient synthesis of complex glycopeptides based on unprotected oligosaccharides

N-Glycopeptides containing 1 to 4 trisaccharide chains, with the carbohydrates vicinal to each other in the multivalent glycopeptides, were efficiently synthesized by using the glycosylated Fmoc-asparagine as a key building block. While the couplings of amino acids with glycopeptides could be achieved in the homogeneous solutions in N-methylpyrrolidinone (NMP) to give excellent yields, all products were conveniently isolated from the reaction mixtures through a precipitation method by using the free carbohydrate chains as phase tags. Commercially available pentafluorophenyl (Pfp) esters of amino acids were employed for the glycopeptide elongation. Longer glycopeptides were constructed by means of a highly convergent synthetic design that is based on the coupling of glycopeptide/peptide fragments. Hydrogen bond interactions between free oligosaccharides were proposed to explain the exceptionally high efficiency of the couplings between two glycosylated building blocks.