CAS 3934-29-0
:acetofluoro-A-D-glucose
Description:
Acetofluoro-A-D-glucose, with the CAS number 3934-29-0, is a derivative of glucose that features a fluorinated acetyl group. This compound is characterized by its structural modifications that enhance its reactivity and solubility compared to unmodified glucose. The presence of the fluorine atom can influence the compound's biological activity, making it of interest in various fields, including medicinal chemistry and biochemistry. Acetofluoro-A-D-glucose may exhibit unique properties such as altered metabolic pathways and interactions with enzymes or receptors due to the fluorine substitution. Additionally, its polar functional groups contribute to its solubility in polar solvents, which is essential for its application in biological systems. The compound's stability, reactivity, and potential applications in drug design or as a biochemical probe are subjects of ongoing research. Overall, acetofluoro-A-D-glucose represents a valuable tool in the study of carbohydrate chemistry and its implications in health and disease.
Formula:C14H19FO9
InChI:InChI=1/C14H19FO9/c1-6(16)20-5-10-11(21-7(2)17)12(22-8(3)18)13(14(15)24-10)23-9(4)19/h10-14H,5H2,1-4H3/t10-,11-,12+,13-,14+/m1/s1
Synonyms:- 2,3,4,6-Tetra-O-Acetyl-Alpha-D-Glucopyranosyl Fluoride
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Found 7 products.
2,3,4,6-Tetra-O-acetyl-α-D-glucopyranosyl Fluoride
CAS:Formula:C14H19FO9Purity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:350.302,3,4,6-Tetra-O-acetyl-α-D-glucopyranosyl fluoride
CAS:Formula:C14H19FO9Purity:97%Color and Shape:SolidMolecular weight:350.2937(2R,3R,4S,5R,6R)-2-(Acetoxymethyl)-6-Fluorotetrahydro-2H-Pyran-3,4,5-Triyl Triacetate
CAS:(2R,3R,4S,5R,6R)-2-(Acetoxymethyl)-6-Fluorotetrahydro-2H-Pyran-3,4,5-Triyl TriacetatePurity:98%Molecular weight:350.29g/mol2,3,4,6-Tetra-O-acetyl-α-D-glucopyranosyl fluoride
CAS:<p>2,3,4,6-Tetra-O-acetyl-a-D-glucopyranosyl fluoride is a halide with the chemical formula of F. It has an axial conformation and is a crystalline solid at room temperature. 2,3,4,6-Tetra-O-acetyl-a-D-glucopyranosyl fluoride reacts with water to form hydrofluoric acid (HF). This compound is an important reagent in carbohydrate analysis because its presence or absence can be used to distinguish between the two anomers of maltose: α-(1→2) and β-(1→4). It also reacts with sodium chloride to give the chloride salt sodium tetrafluoroborate. The molecule has three substituents: a hydroxymethyl group (-OH), a glycosidic oxygen atom (O), and a glucosyl group (-CHO). Watanabe's numbering system for</p>Formula:C14H19FO9Purity:Min. 95%Color and Shape:PowderMolecular weight:350.29 g/mol(2R,3R,4S,5R,6R)-2-(Acetoxymethyl)-6-fluorotetrahydro-2H-pyran-3,4,5-triyl triacetate
CAS:Formula:C14H19FO9Purity:97%Molecular weight:350.2952,3,4,6-Tetra-O-Acetyl-α-D-Glucopyranosyl Fluoride
CAS:<p>2,3,4,6-Tetra-O-acetyl-α-D-glucopyranosyl fluoride is a glycosyl fluoride that inhibits the enzyme glucosidase. This compound has been shown to inhibit peptide degradation and is used in studies of proteolytic enzymes. 2,3,4,6-Tetra-O-acetyl-α-D-glucopyranosyl fluoride has also been used as an inhibitor of carbohydrate metabolism and in the synthesis of glycoproteins.</p>Formula:C14H19O9FPurity:Min. 95%Molecular weight:350.29 g/mol
