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2,3,4,6-Tetra-O-benzyl-a-D-glucopyranose
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2,3,4,6-Tetra-O-benzyl-a-D-glucopyranose

CAS: 6564-72-3

Ref. 3D-MT01011

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Estimated delivery in United States, on Tuesday 18 Feb 2025

Product Information

Name:
2,3,4,6-Tetra-O-benzyl-a-D-glucopyranose
Synonyms:
  • (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)-
Description:

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.

Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Molecular weight:
540.65 g/mol
Formula:
C34H36O6
Purity:
Min. 95%
Color/Form:
White crystals.
MDL:
Melting point:
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Flash point:
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Concentration:
EINECS:
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HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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