134003-35-3

Basic information

• Product Name: pent-4-enyl 2,3,4,6-tetra-O-benzyl-D-glucopyranoside
• Synonyms: pent-4-enyl 2,3,4,6-tetra-O-benzyl-D-glucopyranoside
• CAS NO: 134003-35-3
• Molecular Weight: 608.775
• Mol File: 134003-35-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: pent-4-enyl 2,3,4,6-tetra-O-benzyl-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: pent-4-enyl 2,3,4,6-tetra-O-benzyl-D-glucopyranoside(134003-35-3)
• EPA Substance Registry System: pent-4-enyl 2,3,4,6-tetra-O-benzyl-D-glucopyranoside(134003-35-3)

Safety Data

• Hazardous Substances Data: 134003-35-3(Hazardous Substances Data)

Upstream product

• 109-67-1 1-penten 
• 821-09-0 n-Pent-4-enyl alcohol 
• 100-39-0 benzyl bromide 
• 182074-52-8 pent-4-enyl α,β-D-glucopyranoside 

Downstream Products

• 136755-16-3 N-acetyl-2,3,4,6-tetra-O-benzyl-N-(benzyl-N-benzyloxycarbonyl-L-β-aspartyl)-α-D-glucopyranosylamine 
• 85917-85-7 2,3,4,6-tetra-O-benzyl-N-(O-benzyl-N-benzyloxycarbonyl-L-β-aspartyl)-α-D-glucopyranosylamine 
• 136755-17-4 N-acetyl-2,3,4,6-tetra-O-benzyl-α-D-glucopyranosylamine 
• 4132-26-7 2,3,4,6-tetra-O-benzyl 1,5-anhydro-D-arabino-hex-1-enitol 
• 89025-46-7 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl fluoride 
• 173395-55-6 (3aR,5R,5aS,8aS,8bR)-2,2,7,7-tetramethyl-5-((((3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-3aH-bis[1,3]dioxolo[4,5-b:4',5'-d]pyran 
• 84799-76-8 methyl O-(2,3,4,6-tetra-O-benzyl-D-glucopyranosyl)-(1-4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside 
• 61474-61-1 methyl 2,3,4-tri-O-benzyl-6-O-(2,3,4,6-tetra-O-benzyl-D-glucopyranosyl)-α-D-glucopyranoside 
• 84799-77-9 methyl 2,3,4,6-tetra-O-benzyl-D-glucopyranoside 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 4196-35-4 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl bromide 
• 135080-50-1 (1α,4aβ,8α,8aα)-Decahydro-8-hydroxy-1-naphthyl 2,3,4,6-Tetra-O-benzyl-α-D-Glucopyranoside 

Relevant articles and documents

Synthesis of 2,3,4,6-tetra-O-benzyl-D-glucal on the gram scale. A convenient method for its facile synthesis and subsequent stereoselective cyclopropanation

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An efficient glycosylation protocol with glycosyl ortho-alkynylbenzoates as donors under the catalysis of Ph3PAuOTf

A new and powerful glycosylation protocol with glycosyl ortho-alkynylbenzoates as donors and Ph3PAuOTf as a promoter is disclosed. The donors are readily available and stable; the glycosidic coupling yields are generally excellent; the promotion system is catalytic, neutral, and orthogonal to the known glycosylation conditions.