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

HCID 22887174
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Basic informationNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
53929-38-7
Standard SMILES
O[C@@H]1[C@H](OCc2ccccc2)[C@@H](OCc2ccccc2)[C@@H](OCc2ccccc2)O[C@@H]1COCc1ccccc1
InChIKey
HYZRJGYIUDQFSY-YODGASFJSA-N
Molecular formula
C34H36O6
Average molar mass
540.6 g/mol
Monoisotopic mass
540.25118886

Names & identifiers

Preferred name
Benzyl 2,3,6-tri-O-benzyl-alpha-D-galactopyranoside
IUPAC
(2R,3S,4S,5R,6S)-4,5,6-tris(phenylmethoxy)-2-(phenylmethoxymethyl)oxan-3-ol
English name
Benzyl 2,3,6-Tri-O-benzyl--D-galactopyranoside
Molecular formula
C34H36O6
Molecular weight
540.65

Names & synonyms

53929-38-7Benzyl 2,3,6-tri-O-benzyl-alpha-D-galactopyranoside(2R,3S,4S,5R,6S)-4,5,6-tris(phenylmethoxy)-2-(phenylmethoxymethyl)oxan-3-olorb2941284SCHEMBL7639364DTXSID40628742TSW-00748Benzyl 2,3,6-Tri-O-Benzyl-| inverted exclamation marke-D-Galactopyranoside(2R,3S,4S,5R,6S)-4,5,6-Tris(benzyloxy)-2-((benzyloxy)methyl)tetrahydro-2H-pyran-3-olSureCN7639364, CTK8F7995, AG-F-85926, Benzyl 2,3,6-Tri-O-benzyl-beta-D-galactopyranoside, 53929-38-7Benzyl 2,3,6-Tri-O-benzyl--D-galactopyranosideα-D-Galactopyranoside, phenylmethyl 2,3,6-tris-O-(phenylmethyl)-

Database identifiers

CAS
53929-38-7
PubChem CID
22887174
DTXSID
DTXSID40628742
Nikkaji
J1.929.578H

Properties

Computed structural properties

XLogP
5
Topological polar surface area
66.4 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
6
Rotatable bonds
13
Heavy atoms
40
Formal charge
0
Complexity
665

Physicochemical properties

Boiling point
676.061 · 676.061±55.00 °C(Press: 760.00 Torr)(predicted)
Density
1.222 · 1.222±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
pka
12.922 · 12.922±0.70(predicted)

Chemistry & industry

Applications · 1 item

UsesPhenylmethyl 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].

Suppliers3 total

圣克鲁斯生物技术(上海)有限公司021-60936350 · [email protected]
TORONTO[email protected]
爱必信(上海)生物科技有限公司021-38015121-8802 · [email protected]

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Compound notes

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