2,3,4,6-Tetra-O-benzyl-a-D-glucopyranose
CAS: 6564-72-3
Ref. 3D-MT01011
1kg | To inquire | ||
2kg | To inquire | ||
100g | To inquire | ||
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500g | To inquire |
Product Information
- (2S,3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-ol
- 2, 3, 4, 6-Tetra-O-Benzyl-α-<span class="text-smallcaps">D</span>-glucopyranose
- 2,3,4,6-Tetra-O-benzyl-D-glucofuranose
- 2,3,4,6-Tetra-O-benzyl-alpha-D-glucose
- 2,3,4,6-Tetra-O-benzyl-α-<span class="text-smallcaps">D</span>-glucopyranose
- 2,3,4,6-Tetra-O-benzyl-α-<span class="text-smallcaps">D</span>-glucose
- 2,3,4,6-Tetrakis-O-(phenylmethyl)-α-<span class="text-smallcaps">D</span>-glucopyranose
- Glucopyranose, 2,3,4,6-tetra-O-benzyl-, α-<span class="text-smallcaps">D</span>-
- α-<span class="text-smallcaps">D</span>-Glucopyranose, 2,3,4,6-tetrakis-O-(phenylmethyl)-
2,3,4,6-Tetra-O-benzyl-a-D-glucopyranose is a synthetic derivative of galactose that can be used as a sugar donor in the synthesis of various types of glycosides. It is activated with phosphorus oxychloride and aluminium chloride to yield the corresponding anhydride. The hydroxy group on 2,3,4,6-tetra-O-benzyl-a-D-glucopyranose may be converted to an alkene by condensation with naphthalene or another electrophile. The stereoselective introduction of the hydroxy group using this method provides a valuable tool for chemists who are interested in synthesizing chiral molecules.
Chemical properties
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