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CAS 27851-29-2
:[(3R,4S,5S,6R)-3,4,5,6-tetrabenzyloxytetrahydropyran-2-yl]methanol
Formula:C34H36O6
InChI:InChI=1/C34H36O6/c35-21-30-31(36-22-26-13-5-1-6-14-26)32(37-23-27-15-7-2-8-16-27)33(38-24-28-17-9-3-10-18-28)34(40-30)39-25-29-19-11-4-12-20-29/h1-20,30-35H,21-25H2/t30?,31-,32+,33+,34-/m1/s1
InChI key:HYWPIYGUZWWMDH-BGSSSCFASA-N
SMILES:C1=CC=C(C=C1)CO[C@@H]2[C@H](O[C@H]([C@@H]([C@H]2OCC3=CC=CC=C3)OCC4=CC=CC=C4)OCC5=CC=CC=C5)CO
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Benzyl 2,3,4-Tri-O-benzyl-beta-D-glucopyranoside
CAS:Formula:C34H36O6Purity:min. 95.0 area%(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:540.66Benzyl 2,3,4-tri-O-benzyl-β-D-glucopyranoside
CAS:Benzyl 2,3,4-tri-O-benzyl-β-D-glucopyranosideFormula:C34H36O6Purity:>98%Molecular weight:540.64604((2S,3R,4S,5R,6S)-3,4,5,6-Tetrakis(benzyloxy)tetrahydro-2H-pyran-2-yl)methanol
CAS:Formula:C34H36O6Purity:95%Color and Shape:SolidMolecular weight:540.64601,2,3,4-Tetra-O-benzyl-β-D-glucopyranoside
CAS:1,2,3,4-Tetra-O-benzyl-β-D-glucopyranoside is a prodrug that becomes active after acetylation. It is an endogenous compound that has been shown to inhibit the synthesis of myelin and lipid peroxidation in rat brains. This drug has also been found to be effective in the treatment of amyotrophic lateral sclerosis (ALS). 1,2,3,4-Tetra-O-benzyl-β-D-glucopyranoside is unmodified and does not have any side effects on the nervous system. It can be used for the treatment of Parkinson's disease when combined with levodopa.Formula:C34H36O6Purity:Min. 95%Color and Shape:White Off-White PowderMolecular weight:540.65 g/molBenzyl 2,3,4-Tri-O-benzyl-Beta-D-glucopyranoside
CAS:Controlled ProductApplications Benzyl 2,3,4-Tri-O-benzyl-β-D-glucopyranoside (cas# 27851-29-2) is a compound useful in organic synthesis.
References Wakao, M., et al.: Bioorg. Med. Chem. Lett., 18, 2499 (2008),Formula:C34H36O6Color and Shape:NeatMolecular weight:540.65
