C34H36O6
540.6 g/mol
Research ReagentWarning
2,3,4,6-Tetrakis-O-(phenylmethyl)-alpha-D-glucopyranose
CAS6564-72-3
Category
Research Reagent
Compound Class
Other
Primary Use
Research Compound
This compound is a protected glucose derivative, specifically a fully benzylated form of alpha-D-glucose. It is primarily used as a building block in the chemical synthesis of oligosaccharides, where the benzyl groups serve as protecting groups for the hydroxyl functionalities.
Building block for oligosaccharide synthesisProtected sugar intermediate in carbohydrate chemistry research
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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CAS 6564-72-3
Related Compounds
ReferenceSame Category
Dibenzothiophene, 1-bromo-
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research compound
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research compound
ReferenceSame Category
({[(2-Furylmethyl)(4-methylbenzyl)amino]-carbonothioyl}amino)acetic acid
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research compound
ReferenceSame Category
({[(2-Chlorobenzyl)(2-furylmethyl)amino]-carbonothioyl}amino)acetic acid
CAS656815-90-6
research compound
Referencestereoisomer of
2,3,4,6-tetra-O-benzyl-D-glucopyranose
CAS4132-28-9
pharmaceutical intermediate
Referencestereoisomer of
2,3,4,6-tetrakis-O-(phenylMethyl)-D-Galactopyranose
CAS6386-24-9
research compound
Safety Reference
Warning
H400Very toxic to aquatic life
H410Very toxic to aquatic life with long lasting effects
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
Identifiers
IUPAC Name
(2S,3R,4S,5R,6R)-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-ol
InChIKey
OGOMAWHSXRDAKZ-RUOAZZEASA-N
SMILES
C1=CC=C(C=C1)COC[C@@H]2[C@H]([C@@H]([C@H]([C@H](O2)O)OCC3=CC=CC=C3)OCC4=CC=CC=C4)OCC5=CC=CC=C5
Synonyms (11)
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