| Identification | Back Directory | [Name]
2,3,4,6-TETRA-O-ACETYL-ALPHA-D-MANNOPYRANOSYL FLUORIDE | [CAS]
2823-44-1 | [Synonyms]
acetofluoro-A-D-mannose
acetofluoro-α-d-mannose
ACETOFLUORO-ALPHA-D-MANNOSE
Tetra-O-acetyl-α-D-mannopyranosyl fluoride
2,3,4,6-Tetra-O-acetyl-a-D-mannopyranosyl fluoride
2,3,4,6-tetra-o-acetyl-α-d-mannopyranosyl fluoride
2,3,4,6-Tetra-O-acetyl-α-D-Mannopyranosyl Fluoride
2,3,4,6-TETRA-O-ACETYL-ALPHA-D-MANNOPYRANOSYL FLUORIDE
(2R,3R,4S,5S,6R)-2-(Acetoxymethyl)-6-fluorotetrahydro-2H-pyran-3,4,5-triyl triacetate | [Molecular Formula]
C14H19FO9 | [MDL Number]
MFCD00792706 | [MOL File]
2823-44-1.mol | [Molecular Weight]
350.29 |
| Chemical Properties | Back Directory | [Melting point ]
68-69 °C | [Boiling point ]
374.8±42.0 °C(Predicted) | [density ]
1.30±0.1 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,2-8°C | [form ]
Powder | [color ]
White to Off-white |
| Hazard Information | Back Directory | [Uses]
Acetofluoro-α-D-mannose 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 |
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