402758-94-5

Basic information

• Product Name: methyl 2-O-benzyl-5-O-t-butyldiphenylsilyl-3-O-(3,5-di-O-benzyl-α-D-arabinofuranosyl)-α-D-arabinofuranoside
• Synonyms: methyl 2-O-benzyl-5-O-t-butyldiphenylsilyl-3-O-(3,5-di-O-benzyl-α-D-arabinofuranosyl)-α-D-arabinofuranoside
• CAS NO: 402758-94-5
• Molecular Weight: 805.053
• Mol File: 402758-94-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 2-O-benzyl-5-O-t-butyldiphenylsilyl-3-O-(3,5-di-O-benzyl-α-D-arabinofuranosyl)-α-D-arabinofuranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-O-benzyl-5-O-t-butyldiphenylsilyl-3-O-(3,5-di-O-benzyl-α-D-arabinofuranosyl)-α-D-arabinofuranoside(402758-94-5)
• EPA Substance Registry System: methyl 2-O-benzyl-5-O-t-butyldiphenylsilyl-3-O-(3,5-di-O-benzyl-α-D-arabinofuranosyl)-α-D-arabinofuranoside(402758-94-5)

Safety Data

• Hazardous Substances Data: 402758-94-5(Hazardous Substances Data)

Upstream product

• 402758-78-5 p-cresyl 2-O-benzoyl-3,5-di-O-benzyl-1-thio-α-D-arabinofuranoside 
• 402758-84-3 methyl 2-O-benzyl-5-O-(tert-butyldiphenyl)silyl-α-D-arabinofuranoside 
• 402758-86-5 methyl 2-O-benzoyl-3,5-di-O-benzyl-α-D-arabinofuranoside 
• 402758-82-1 methyl 2-O-benzyl-α-D-arabinofuranoside 
• 329360-22-7 1-O-methyl-3,5-di-O-benzyl-α-D-arabinofuranose 
• 164454-52-8 methyl 3,5-O-(tetraisopropylsiloxane-1,3-diyl)-α-D-arabinofuranoside 
• 100-39-0 benzyl bromide 
• 402758-93-4 methyl 2-O-benzyl-5-O-t-butyldiphenylsilyl-3-O-(2-O-benzoyl-3,5-di-O-benzyl-α-D-arabinofuranosyl)-α-arabinofuranoside 

Downstream Products

• 402758-95-6 methyl 2-O-benzyl-5-O-t-butyldiphenylsilyl-3-O-(3,5-di-O-benzyl-2-O-(2,3,5-tri-O-benzyl-β-D-arabinofuranosyl)-α-D-arabinofuranosyl)-α-D-arabinofuranoside 

Relevant articles and documents

Arabinofuranosides from mycobacteria: Synthesis of a highly branched hexasaccharide and related fragments containing β-arabinofuranosyl residues

The synthesis of 11 oligosaccharides (4-14) containing β-arabinofuranosyl residues is reported. The glycans are all fragments of two polysaccharides, arabinogalactan and lipoarabinomannan, which are found in the cell wall complex of mycobacteria. In the preparation of the targets, the key step was a low-]temperature glycosylation reaction that installed the β-arabinofuranosyl residues with good to excellent stereocontrol.