369641-39-4

Basic information

• Product Name: allyl (2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-(1->2)-(3,4,6-tri-O-benzoyl-α-D-mannopyranosyl)-(1->2)-3,4,6-tri-O-benzoyl-α-D-mannopyranoside
• Synonyms: allyl (2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-(1->2)-(3,4,6-tri-O-benzoyl-α-D-mannopyranosyl)-(1->2)-3,4,6-tri-O-benzoyl-α-D-mannopyranoside
• CAS NO: 369641-39-4
• Molecular Weight: 1585.59
• Mol File: 369641-39-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: allyl (2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-(1->2)-(3,4,6-tri-O-benzoyl-α-D-mannopyranosyl)-(1->2)-3,4,6-tri-O-benzoyl-α-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: allyl (2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-(1->2)-(3,4,6-tri-O-benzoyl-α-D-mannopyranosyl)-(1->2)-3,4,6-tri-O-benzoyl-α-D-mannopyranoside(369641-39-4)
• EPA Substance Registry System: allyl (2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-(1->2)-(3,4,6-tri-O-benzoyl-α-D-mannopyranosyl)-(1->2)-3,4,6-tri-O-benzoyl-α-D-mannopyranoside(369641-39-4)

Safety Data

• Hazardous Substances Data: 369641-39-4(Hazardous Substances Data)

Upstream product

• 324041-21-6 allyl (3,4,6-tri-O-benzoyl-α-D-mannopyranosyl)-(1->2)-3,4,6-tri-O-benzoyl-α-D-mannopyranoside 
• 183901-63-5 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl trichloroacetimidate 

Downstream Products

• 1197987-95-3 3-thioacetoxypropyl (2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-(1->2)-(3,4,6-tri-O-benzoyl-α-D-mannopyranosyl)-(1->2)-3,4,6-tri-O-benzoyl-α-D-mannopyranoside 

Relevant articles and documents

DNA-templated homo- and heterodimerization of peptide nucleic acid encoded oligosaccharides that mimick the carbohydrate epitope of HIV

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Highly efficient synthesis of the mannose nonasaccharide of the N-glycan expressed on the HIV glycoprotein gp 120

A highly concise and effective synthesis of the mannose nonasaccharide of the glycan expressed on the HIV protein gp 120 was achieved via TMSOTf promoted selective 6-glycosylation of a tetrasaccharide 4,6-diol acceptor with a pentasaccharide donor followed by deprotection. The pentasaccharide was constructed by selective 3,6-diglycosylation of 1,2-O-ethylidene-β-D-mannopyranose with 2-O-acetyl-3,4,6-tri-O-benzoyl-α-D-mannopyranosyl-(1→2)-3,4,6- tri-O-benzoyl-α-D-mannopyranosyl trichloroimidate while the tetrasaccharide was obtained by selective 3-O-glycosylation of allyl 4,6-O-benzilidene-α-D-mannopyranoside with 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl-(1→2)-3,4,6-tri-O- benzoyl-α-D-mannopyranosyl-(1→2)-3,4,6-tri-O-benzoyl-α-D- mannopyranosyl trichloroimidate.