65827-59-0

Basic information

• Product Name: 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl chloride
• Synonyms: 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl chloride
• CAS NO: 65827-59-0
• Molecular Weight: 511.015
• Mol File: 65827-59-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl chloride(65827-59-0)
• EPA Substance Registry System: 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl chloride(65827-59-0)

Safety Data

• Hazardous Substances Data: 65827-59-0(Hazardous Substances Data)

Upstream product

• 83-87-4 D-Mannose pentaacetate 
• 3254-16-8 3,4,6-tri-O-acetyl-1,2-O-(1-methoxyethylidene)-β-D-mannopyranose 
• 68567-54-4 1,2-di-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranoside 
• 68681-00-5 3,4,6-tri-O-benzyl-1,2-O-<1-(R)-methoxyethylidene>-β-D-mannopyranose 

Downstream Products

• 141990-25-2 C₁₃₉H₁₄₆O₂₈ 
• 143706-45-0 4-penten-1-yl 2-O-acetyl-2,3,6-tri-O-benzyl-α-D-glucopyranoside 
• 68594-09-2 C₆₅H₇₄O₁₈ 
• 74372-90-0 1,2-anhydro-3,4,6-tri-O-benzyl-β-D-mannopyranose 
• 543698-61-9 ethyl O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->6)-2,3,4-tri-O-benzyl-1-thio-α-D-mannopyranoside 
• 1389321-10-1 C₄₀H₄₅NO₉ 
• 1389321-13-4 C₆₅H₇₁NO₁₃ 
• 1389321-12-3 C₆₇H₇₃NO₁₄ 
• 1389321-11-2 C₃₈H₄₃NO₈ 

Relevant articles and documents

First total synthesis of a GPI-anchored peptide

A GPI-anchored dipeptide of sperm CD52 antigen was prepared through a convergent synthesis. First, the dipeptide with its C-terminus free and the GPI with its nonreducing end phosphoeth-anolamine bearing a free amino group were synthesized separately. Then, the two building blocks were coupled with use of EDC/HOBt as the condensation reagent. Finally, the GPI-anchored peptide was deprotected to give the target molecule 1.

SYNTHETIC STUDIES ON CELL SURFACE GLYCANS 3 BRANCHING PENTASACCHARIDES OF GLYCOPROTEIN

Synthetic routes for the branching pentasaccharides 4 and 5 of glycoproteins are described in a regio- and stereo-controlled way.