Basic information
- CAS
141019-70-7- Standard SMILES
CC(=O)N[C@@H]1[C@H](OCc2ccccc2)O[C@@H](COC(=O)c2ccccc2)[C@@H](O)[C@H]1OC(=O)c1ccccc1- InChIKey
MYVKGGKJMHXHHZ-LGUFPPMKSA-N- Molecular formula
- C29H29NO8
- Average molar mass
- 519.5 g/mol
- Monoisotopic mass
- 519.18931688
Names & identifiers
- Preferred name
- Benzyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-alpha-L-galactopyranoside
- IUPAC
- [(2S,3S,4S,5S,6R)-5-acetamido-4-benzoyloxy-3-hydroxy-6-phenylmethoxyoxan-2-yl]methyl benzoate
- English name
- Benzyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-alpha-D-galactopyranoside
- Molecular formula
- C29H29NO8
- Molecular weight
- 519.54
Names & synonyms
141019-70-7Benzyl 2-Acetamido-3,6-di-O-benzoyl-2-deoxy-alpha-D-galactopyranosideBENZYL 2-ACETAMIDO-3,6-DI-O-BENZOYL-2-DEOXY-A-D-GALACTOPYRANOSIDEDTXSID20849498((2R,3R,4R,5R,6S)-5-Acetamido-4-(benzoyloxy)-6-(benzyloxy)-3-hydroxytetrahydro-2H-pyran-2-yl)methyl benzoateAKOS025294489MB04587Benzyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-alpha-L-galactopyranosideBenzyl 2-Acetamido-3,6-di-O-benzoyl-2-deoxy-α-D-galactopyranosideBenzyl-2-acetamido-3,6-di-O-benzoyl-2-desoxy-α-D-galactopyranosidPhenylMethyl 2-(AcetylaMino)-2-deoxy-α-D-galactopyranoside 3,6-Dibenzoateα-D-Galactopyranoside, phenylmethyl 2-(acetylamino)-2-deoxy-, 3,6-dibenzoate
Show more names
Benzyl 2-Acetamido-3,6-di-O-benzoyl-2-deoxy-α-D-galactopyranoside, CAS 141019-70-7
Database identifiers
Properties
Computed structural properties
- XLogP
- 3.4
- Topological polar surface area
- 120 Ų
- Hydrogen bond donors
- 2
- Hydrogen bond acceptors
- 8
- Rotatable bonds
- 11
- Heavy atoms
- 38
- Formal charge
- 0
- Complexity
- 773
Physicochemical properties
- Boiling point
- 724.7 · 724.7±60.0 °C(Predicted)
- Density
- 1.32 · 1.32±0.1 g/cm3(Predicted)
- solubility
- DMSO, Hot Ethanol, Methanol
- form
- Solid
- pka
- 12.54 · 12.54±0.70(Predicted)
- color
- White
Chemistry & industry
Applications
UsesBenzyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-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].
Upstream & downstream products
Downstream products
Suppliers5 total
凯试（上海）科技有限公司021-50135380 · [email protected]
安耐吉化学&3A（安徽泽升科技股份有限公司）400-0056266 · [email protected]
深圳聚合生化科技有限公司+86-400-002-6226 13028896684 · [email protected]
Alchem Pharmtech,Inc.8485655694 · [email protected]
北京百灵威科技有限公司18210857532 18210857532 · [email protected]
Related reactions
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Compound notes
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