569352-00-7

Basic information

• Product Name: α-benzyl-β-carboxy-(methyl 2,3,4-tri-O-triethylsilyl-α-D-mannopyranos-6-O-yl)-N-9-fluorenylmethoxycarbonyl-L-aspartic acid
• Synonyms: α-benzyl-β-carboxy-(methyl 2,3,4-tri-O-triethylsilyl-α-D-mannopyranos-6-O-yl)-N-9-fluorenylmethoxycarbonyl-L-aspartic acid
• CAS NO: 569352-00-7
• Molecular Weight: 964.429
• Mol File: 569352-00-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: α-benzyl-β-carboxy-(methyl 2,3,4-tri-O-triethylsilyl-α-D-mannopyranos-6-O-yl)-N-9-fluorenylmethoxycarbonyl-L-aspartic acid(CAS DataBase Reference)
• NIST Chemistry Reference: α-benzyl-β-carboxy-(methyl 2,3,4-tri-O-triethylsilyl-α-D-mannopyranos-6-O-yl)-N-9-fluorenylmethoxycarbonyl-L-aspartic acid(569352-00-7)
• EPA Substance Registry System: α-benzyl-β-carboxy-(methyl 2,3,4-tri-O-triethylsilyl-α-D-mannopyranos-6-O-yl)-N-9-fluorenylmethoxycarbonyl-L-aspartic acid(569352-00-7)

Safety Data

• Hazardous Substances Data: 569352-00-7(Hazardous Substances Data)

Upstream product

• 86060-83-5 N-(9-fluorenylmethoxycarbonyl)-L-aspartyl α-benzyl ester 
• 569351-99-1 methyl 2,3,4-tri-O-triethylsilyl-α-D-mannopyranoside 
• 569351-98-0 methyl 2,3,4-tri-O-triethylsilyl-6-O-benzyl-α-D-mannopyranoside 
• 23392-33-8 methyl 6-O-benzyl-α-D-mannopyranoside 
• 3162-96-7 methyl-4,6-O-phenylmethylene-α-D-mannopyranoside 
• 617-04-9 (2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-methoxytetrahydro-2H-pyran-3,4,5-triol 

Relevant articles and documents

Solid phase peptide templated glycosidic bond formation

Glycosylation reactions performed between a glycosyl donor and acceptor covalently linked to a peptide template both in the solution and solid phase give similar yields and product distributions. The adoption of a solid phase approach opens the way for the synthesis of libraries of peptide templates in an attempt to screen for particular peptide sequences that effect complete regio-and stereochemical control during glycosidic bond formation, whilst the use of second generation donors allows the possibility of an iterative approach.