1,3,4,6-Tetra-O-acetyl-2-deoxy-2-trifluoracetamido-D-glucose
1,3,4,6-Tetra-O-acetyl-2-deoxy-2-trifluoracetamido-D-glucose Basic information
- Product Name:
- 1,3,4,6-Tetra-O-acetyl-2-deoxy-2-trifluoracetamido-D-glucose
- Synonyms:
-
- 1,3,4,6-Tetra-O-acetyl-2-deoxy-2-trifluoracetamido-D-glucose
- Acetic Acid 2,5-Diacetoxy-6-acetoxymethyl-3-(2,2,2-trifluoro-acetylamino)-tetrahydro-pyran- 4-yl Ester
- 1,3,4,6-tetra-O-acetyl-2-deoxy-2-trifluoracetamido-β-D-glucopyranoside
- β-D-Glucopyranose, 2-deoxy-2-[(2,2,2-trifluoroacetyl)amino]-, 1,3,4,6-tetraacetate
- CAS:
- 7139-63-1
- MF:
- C16H20F3NO10
- MW:
- 443.3259096
- Product Categories:
-
- Carbohydrates & Derivatives
- 13C & 2H Sugars
- Mol File:
- 7139-63-1.mol
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1,3,4,6-Tetra-O-acetyl-2-deoxy-2-trifluoracetamido-D-glucose Chemical Properties
- Melting point:
- 164-165°C
- Boiling point:
- 495.2±45.0 °C(Predicted)
- Density
- 1.40±0.1 g/cm3(Predicted)
- pka
- 8.34±0.70(Predicted)
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1,3,4,6-Tetra-O-acetyl-2-deoxy-2-trifluoracetamido-D-glucose Usage And Synthesis
Chemical Properties
Off-White Solid
Uses
1,3,4,6-Tetra-O-acetyl-2-deoxy-2-trifluoracetamido-D-glucose 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].
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
1,3,4,6-Tetra-O-acetyl-2-deoxy-2-trifluoracetamido-D-glucoseSupplier
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