117841-64-2

Basic information

• Product Name: (pent-4′-enyl) 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside
• Synonyms: (pent-4′-enyl) 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside
• CAS NO: 117841-64-2
• Molecular Weight: 608.775
• Mol File: 117841-64-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (pent-4′-enyl) 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: (pent-4′-enyl) 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside(117841-64-2)
• EPA Substance Registry System: (pent-4′-enyl) 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside(117841-64-2)

Safety Data

• Hazardous Substances Data: 117841-64-2(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 123487-56-9 pent-4-enyl 3,4,6-tri-O-benzyl-α-D-mannopyranoside 
• 150772-52-4 n-pent-4-enyl 2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranoside 
• 163039-18-7 (3aS,5R,6S,7S,7aS)-5-Hydroxymethyl-2-pent-4-enyloxy-2-phenyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran-6,7-diol 
• 125392-62-3 3,4,6-tri-O-benzyl-β-D-mannopyranose 1,2-(pent-4-enyl orthobenzoate) 
• 123487-55-8 3,4,6-tri-O-benzoyl-β-D-mannopyranose 1,2-(pent-4-enyl orthobenzoate) 
• 821-09-0 n-Pent-4-enyl alcohol 
• 3879-79-6 (2R,3R,4S,5S,6S)-3,4,5-tris(benzyloxy)-2-((benzyloxy)methyl)-6-methoxytetrahydro-2H-pyran 
• 38184-10-0 phenyl 2,3,4,6-tetra-O-benzyl-1-thio-α-D-mannopyranoside 

Downstream Products

• 297747-21-8 3,6-di-O-allyl-1-O-methyl-4-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranoside 
• 297747-20-7 3,6-di-O-allyl-1-O-methyl-2-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranoside 
• 1198083-85-0 C₆₄H₆₀O₁₄ 
• 1198083-84-9 C₆₄H₆₆O₁₁ 
• 78153-79-4 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl fluoride 
• 55094-26-3 methyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1→6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside 

Relevant articles and documents

Stereocontrolled glycoside synthesis by activation of glycosyl sulfone donors with scandium(III) triflate

The activation of aryl glycosyl sulfone donors has been achieved using scandium(iii) triflate and has led to the selective preparation of α-mannosides resulting from a post-glycosylation anomerization.

Synthesis of a key Mycobacterium tuberculosis biosynthetic phosphoinositide intermediate

Regioselective mannosylations of a myoinositol acceptor diol are readily achieved by Lewis acid mediated iodinolysis of n-pentenyl ortho-esters. The procedure affords a psuedotrisaccharide to which the phosphoglyceryl and other lipid residues are added le

Studies related to synthesis of glycophosphatidylinositol membrane-bound protein anchors. 5. n-pentenyl ortho esters for mannan components

Procedures for rapid assembly of multigram amounts of mannan components have been examined. Although these studies are reported in the context of the mannan moiety of the glycan anchors of membrane-bound glycoproteins, the procedures should be applicable