1190749-46-2

Basic information

• Product Name: 3-azidopropyl 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl-(1->6)-[2,3,5-tri-O-benzoyl-α-L-arabinofuranosyl-(1->3)]-2,4-di-O-benzoyl-β-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-β-D-galactopyranoside
• Synonyms: 3-azidopropyl 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl-(1->6)-[2,3,5-tri-O-benzoyl-α-L-arabinofuranosyl-(1->3)]-2,4-di-O-benzoyl-β-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-β-D-galactopyranoside
• CAS NO: 1190749-46-2
• Molecular Weight: 1968.95
• Mol File: 1190749-46-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-azidopropyl 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl-(1->6)-[2,3,5-tri-O-benzoyl-α-L-arabinofuranosyl-(1->3)]-2,4-di-O-benzoyl-β-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-β-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 3-azidopropyl 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl-(1->6)-[2,3,5-tri-O-benzoyl-α-L-arabinofuranosyl-(1->3)]-2,4-di-O-benzoyl-β-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-β-D-galactopyranoside(1190749-46-2)
• EPA Substance Registry System: 3-azidopropyl 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl-(1->6)-[2,3,5-tri-O-benzoyl-α-L-arabinofuranosyl-(1->3)]-2,4-di-O-benzoyl-β-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-β-D-galactopyranoside(1190749-46-2)

Safety Data

• Hazardous Substances Data: 1190749-46-2(Hazardous Substances Data)

Upstream product

• 1439439-37-8 3-azidopropyl 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl-(1→6)-2,4-di-O-benzoyl-1-thio-β-D-galactopyranosyl-(1→6)-2,3,4-tri-O-benzoyl-β-D-galactopyranoside 
• 1190749-45-1 3-azidopropyl 2,3,5-tri-O-benzoyl-α-L-arabinofuranosyl-(1->3)-2,4-di-O-benzoyl-β-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-β-D-galactopyranoside 
• 62774-33-8 phenyl 2,3,4,6-tetra-O-benzoyl-1-thio-β-D-galactopyranoside 

Relevant articles and documents

One-pot synthesis of branched oligosaccharides by use of galacto- and mannopyranosyl thioglycoside diols as key glycosylating agents

We describe in this paper the efficient four-component one-pot synthesis of three fully protected oligosaccharides 22, 36, and 50 with di-branched structures by employing d-galacto- and mannopyranosyl thioglycoside diols as central glycosylating agents. After global deprotection, they were converted respectively into the 3-aminopropyl linker-containing free oligosaccharide fragments 14, 24, and 38 structurally related to cell wall oligosaccharides from Atractylodes lancea DC, the marine fungus Lineolata rhizophorae and pathogenic Mycobacterium tuberculosis. The 3-aminopropyl linker at the anomeric carbon can enable conjugation of these synthetic oligomers to a suitable protein carrier. This journal is The Royal Society of Chemistry 2013.