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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 22887174Generated: November 2, 2026

Benzyl 2,3,6-tri-O-benzyl-alpha-D-galactopyranoside

Benzyl 2,3,6-Tri-O-benzyl--D-galactopyranoside · α-D-Galactopyranoside, phenylmethyl 2,3,6-tris-O-(phenylmethyl)-

https://huagongshe.com/en/chemical/22887174

Benzyl 2,3,6-tri-O-benzyl-alpha-D-galactopyranoside molecular structure

Identifiers & Physical Properties

CAS No.53929-38-7
Molecular formulaC34H36O6
Average molar mass540.6 g/mol
Monoisotopic mass540.25118886 g/mol
SMILESO[C@@H]1[C@H](OCc2ccccc2)[C@@H](OCc2ccccc2)[C@@H](OCc2ccccc2)O[C@@H]1COCc1ccccc1
InChIKeyHYZRJGYIUDQFSY-YODGASFJSA-N
PubChem CID22887174
DTXSIDDTXSID40628742

Chemical & Physical Properties

XLogP5
Topological polar surface area66.4
Hydrogen bond donors1
Hydrogen bond acceptors6
Rotatable bonds13
Heavy atoms40
Formal charge0
Complexity665
Boiling point676.061±55.00 °C(Press: 760.00 Torr)(predicted)
Density1.222±0.10 g/cm3(Temp: 25 °CPress: 760 Torr)(predicted)
pKa (acidity coefficient)12.922±0.70(predicted)

Applications & Uses

Uses

Phenylmethyl 2,3,6-tris-O-(phenylmethyl)-α-D-galactopyranoside is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology[1].