Methyl2-acetamido-3,6-di-O-benzyl-2-deoxy-a-D-glucopyranoside
Methyl2-acetamido-3,6-di-O-benzyl-2-deoxy-a-D-glucopyranoside Basic information
- Product Name:
- Methyl2-acetamido-3,6-di-O-benzyl-2-deoxy-a-D-glucopyranoside
- Synonyms:
-
- Methyl2-acetamido-3,6-di-O-benzyl-2-deoxy-a-D-glucopyranoside
- Methyl 2-(AcetylaMino)-2-deoxy-3,6-bis-O-(phenylMethyl)-α-D-glucopyranoside
- Methyl 2-Acetamido-2-deoxy-3,6-di-O-benzyl-α-D-glucopyranoside
- α-D-Glucopyranoside, methyl 2-(acetylamino)-2-deoxy-3,6-bis-O-(phenylmethyl)-
- CAS:
- 85193-92-6
- MF:
- C23H29NO6
- MW:
- 415.48
- Product Categories:
-
- Carbohydrates & Derivatives
- Mol File:
- 85193-92-6.mol
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Methyl2-acetamido-3,6-di-O-benzyl-2-deoxy-a-D-glucopyranoside Chemical Properties
- Boiling point:
- 623.7±55.0 °C(Predicted)
- Density
- 1.22±0.1 g/cm3(Predicted)
- pka
- 12.94±0.70(Predicted)
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Methyl2-acetamido-3,6-di-O-benzyl-2-deoxy-a-D-glucopyranoside Usage And Synthesis
Uses
Methyl 2-acetamido-2-deoxy-3,6-di-O-benzyl-α-D-glucopyranosideis 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].
References
[1] Varki A, et al editors. Essentials of Glycobiology [Internet]. 4th ed. Cold Spring Harbor (NY): Cold Spring Harbor Laboratory Press; 2022. PMID:35536922
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