Description

2-Phenylmethoxyoxane-3,4,5-triol (CAS No. 7473-38-3) is a high-purity carbohydrate derivative extensively utilized in biochemical and pharmaceutical research. With the molecular formula C₁₂H₁₆O₅, this compound is a benzyl-protected arabinopyranoside, offering exceptional stability and reactivity for glycosylation studies. Ideal for researchers focusing on glycochemistry, enzymatic synthesis, or drug development, this product is rigorously tested for purity (≥95% by HPLC) and consistency. Available in crystalline or lyophilized form, it is packaged under inert conditions to ensure long-term stability. Each batch is accompanied by comprehensive analytical data, including NMR and MS spectra, to guarantee reproducibility in your experiments.

Properties

• CAS Number: 7473-38-3
• Complexity: 229
• IUPAC Name: 2-benzyloxytetrahydropyran-3,4,5-triol
• InChI: InChI=1S/C12H16O5/c13-9-7-17-12(11(15)10(9)14)16-6-8-4-2-1-3-5-8/h1-5,9-15H,6-7H2
• InChI Key: XUGMDBJXWCFLRQ-UHFFFAOYSA-N
• Exact Mass: 240.09977361
• Molecular Formula: C12H16O5
• Molecular Weight: 240.25
• SMILES: C1C(C(C(C(O1)OCC2=CC=CC=C2)O)O)O
• Topological: 79.2
• Monoisotopic Mass: 240.09977361
• Synonyms: NSC2561, 7473-38-3, 2-phenylmethoxyoxane-3,4,5-triol, Benzyl -D-arabinopyranoside, Benzyl beta-D-ribopyranoside, Benzyl beta-L-ribopyranoside, MLS000736490, benzyl beta-l-arabinopyranoside, benzyl pentopyranoside, (2S,3R,4S,5R)-2-(Benzyloxy)tetrahydro-2H-pyran-3,4,5-triol, 70797-93-2, MFCD00225631, 61134-26-7, Oprea1_820628, CHEMBL1710955, SCHEMBL14356311, HMS2819E07, NSC170150, NSC231837, NSC400277, NSC-170150, NSC-231837, NSC-400277, SB47916, SB49542, BENZYL .BETA.-D-ARABINOPYRANOSIDE, NCI60_002061, SMR000528040, SY124816

This compound is widely employed as a key intermediate in the synthesis of complex glycoconjugates and nucleoside analogs. Researchers utilize it in glycosylation reactions to study enzyme mechanisms or develop novel carbohydrate-based therapeutics. Its benzyl-protected structure makes it particularly valuable in selective deprotection strategies for oligosaccharide assembly. Additionally, it serves as a reference standard in chromatographic and mass spectrometric analyses of sugar derivatives.

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