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| | 2,3,4,6-Tetra-O-acetyl-alpha-D-mannopyranosyl fluoride Basic information |
| Product Name: | 2,3,4,6-Tetra-O-acetyl-alpha-D-mannopyranosyl fluoride | | Synonyms: | ACETOFLUORO-ALPHA-D-MANNOSE;acetofluoro-A-D-mannose;2,3,4,6-tetra-o-acetyl-α-d-mannopyranosyl fluoride;acetofluoro-α-d-mannose;2,3,4,6-Tetra-O-acetyl-a-D-mannopyranosyl fluoride;Tetra-O-acetyl-α-D-mannopyranosyl fluoride;(2R,3R,4S,5S,6R)-2-(Acetoxymethyl)-6-fluorotetrahydro-2H-pyran-3,4,5-triyl triacetate;α-D-Mannopyranosyl fluoride, 2,3,4,6-tetraacetate | | CAS: | 2823-44-1 | | MF: | C14H19FO9 | | MW: | 350.29 | | EINECS: | | | Product Categories: | | | Mol File: | 2823-44-1.mol |  |
| | 2,3,4,6-Tetra-O-acetyl-alpha-D-mannopyranosyl fluoride Chemical Properties |
| 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 |
| | 2,3,4,6-Tetra-O-acetyl-alpha-D-mannopyranosyl fluoride Usage And Synthesis |
| 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 |
| | 2,3,4,6-Tetra-O-acetyl-alpha-D-mannopyranosyl fluoride Preparation Products And Raw materials |
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