20888-02-2

Basic information

• Product Name: 1,6-anhydro-2,3,4-tri-O-benzyl-β-D-mannopyranose
• Synonyms: 1,6-anhydro-2,3,4-tri-O-benzyl-β-D-mannopyranose
• CAS NO: 20888-02-2
• Molecular Weight: 432.516
• Mol File: 20888-02-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1,6-anhydro-2,3,4-tri-O-benzyl-β-D-mannopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1,6-anhydro-2,3,4-tri-O-benzyl-β-D-mannopyranose(20888-02-2)
• EPA Substance Registry System: 1,6-anhydro-2,3,4-tri-O-benzyl-β-D-mannopyranose(20888-02-2)

Safety Data

• Hazardous Substances Data: 20888-02-2(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 14168-65-1 mannosan 
• 1253191-75-1 propargyl 2,3,4-tri-O-benzoyl α-D-mannopyranoside 
• 1253191-79-5 C₆₄H₆₆O₁₁ 
• 530-26-7 D-Mannose 
• 1344980-46-6 C₅₀H₅₄O₇Si 
• 34212-64-1 methyl 2,3,4-tri-O-benzyl-α-D-mannopyranoside 
• 1198083-98-5 C₃₀H₃₂O₆ 

Downstream Products

• 67227-89-8 1,6-anhydro-3,4-di-O-benzyl-β-D-mannopyranoside 
• 66963-73-3 1,6-anhydro-3,4-di-O-benzyl-2-O-benzoyl-β-D-mannopyranoside 
• 118895-69-5 Benzoic acid (1R,2R,3S,4S,5R)-2,4-bis-benzyloxy-6,8-dioxa-bicyclo[3.2.1]oct-3-yl ester 
• 97292-02-9 1,6-anhydro-3,4-di-O-benzyl-2-O-<(trifluoromethyl)sulfonyl>-β-D-mannopyranose 
• 118895-75-3 1,6-anhydro-2-O-benzoyl-4-O-benzyl-3-O-methyl-β-D-mannopyranose 
• 118895-77-5 1,6-anhydro-2-O-benzoyl-3-O-benzyl-4-O-methyl-β-D-mannopyranose 
• 118895-79-7 1,6-anhydro-3-O-benzoyl-4-O-benzyl-2-O-methyl-β-D-mannopyranose 
• 118895-70-8 1,6-anhydro-2,4-di-O-benzyl-3-O-methyl-β-D-mannopyranose 
• 118895-73-1 1,6-anhydro-3,4-di-O-benzyl-2-O-methyl-β-D-mannopyranose 
• 118895-78-6 1,6-anhydro-4-O-benzyl-2-O-methyl-β-D-mannopyranose 
• 118895-74-2 1,6-anhydro-4-O-benzyl-3-O-methyl-β-D-mannopyranose 
• 55682-48-9 1,6-anhydro-2-azido-3,4-di-O-benzyl-2-deoxy-D-glucopyranose 
• 55682-57-0 1,6-anhydro-2-azido-3-O-benzyl-2-deoxy-β-D-glucopyranose 
• 79522-92-2 Benzyl-6-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranosid 

Relevant articles and documents

Oligosaccharide compound and its manufacture and its intermediate

The purpose of the present invention is to provide an oligosaccharide with high versatility that can produce a protected sulfate oligosaccharide that can become a manufacturing intermediate of polysulfated hyaluronic acid, and to provide a manufacturing method therefor and an intermediate thereof. Position 2 amino groups in glucosamine, galactosamine, and the like can react with saccharide receptors having an electron attracting group such as glucuronic acid and protected sulfate groups, by using a saccharide donor protected by a specific protective group.

Gold-catalyzed glycosidations: Synthesis of 1,6-anhydro saccharides

Various 1,6-anhydro sugars are synthesized utilizing salient features of gold-catalyzed glycosidations. All the reactions occurred under mild conditions in the presence of 7 mol % of AuBr3 enabling easy synthesis of 1,6-anhydro sugars from corr

Studies related to synthesis of glycophosphatidylinositol membrane-bound protein anchors. 6. Convergent assembly of subunits

Glycophosphatidylinositol anchors of membrane-bound proteins are thought to comprise a common pentasaccharide core containing mannan, glucosamine, and inositol residues. A synthetic route to this core is described. In addition, the complete heptasaccharide moiety of the rat brain Thy-1 membrane anchor, the first mammalian membrane anchor to be characterized, has been synthesized. In the case of the Thy-1 anchor, the synthetic plan is based on three building blocks comprising glucosamine-inositol, galactosamine-mannose, and trimannan residues. Although glycosyl donors other than n-pentenyl glycosides (NPGs) have been used in preparing each of these building blocks, the final assembly of the heptasaccharide utilizes NPGs as the only glycosyl donors. The mildness of the conditions for these coupling reactions has allowed us to make provisions for subsequent installation of the three phosphodiester units.