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  • 2823-46-3 , 氟代-β-D-吡喃葡萄糖四乙酸酯, CAS: 2823-46-3
2823-46-3 , 氟代-β-D-吡喃葡萄糖四乙酸酯, CAS: 2823-46-3

2823-46-3 , 氟代-β-D-吡喃葡萄糖四乙酸酯, CAS: 2823-46-3

2823-46-3 , β-D-Glucopyranosyl fluoride tetraacetate ,
氟代-β-D-吡喃葡萄糖四乙酸酯,
CAS: 2823-46-3
C14H19FO9 / 350.29
MFCD01862267

2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl fluoride

 氟代-β-D-吡喃葡萄糖四乙酸酯, 

Beta-D-Glucopyranosyl fluoride tetraacetate is a complex chemical compound with a variety of physical, chemical, and biological properties. It has become an essential element in scientific research and is actively being explored for its potential applications in numerous fields.

Definition and Background:

Beta-D-Glucopyranosyl fluoride tetraacetate is a combination of sugar derivatives and fluorine that is widely used in organic chemistry. It is commonly used for glycosylation reactions, where it helps in the formation of glycosidic bonds. Beta-D-Glucopyranosyl fluoride tetraacetate is used to study the stereochemistry of sugar molecules, glycoprotein synthesis, and the development of new drugs and treatments.

Synthesis and Characterization:

There are several methods for the synthesis of Beta-D-Glucopyranosyl fluoride tetraacetate. The most commonly used method involves the reaction of glucose with sulfur tetrafluoride in the presence of acetic anhydride. The purity of the compound can be determined by Nuclear Magnetic Resonance (NMR) spectroscopy, High-Performance Liquid Chromatography (HPLC), and Mass Spectrometry (MS).

Analytical Methods:

Several analytical methods are used to study the properties and behavior of Beta-D-Glucopyranosyl fluoride tetraacetate. NMR spectroscopy is used to determine the purity and structure of the compound. Mass spectrometry and HPLC are used to determine the molecular weight and composition of the compound.

Biological Properties:

Beta-D-Glucopyranosyl fluoride tetraacetate has several biological properties that make it useful in medical research. The compound has been shown to have antitumor properties and can be used to target cancer cells. It also has antiviral properties and can be used to fight viral infections.

Toxicity and Safety in Scientific Experiments:

Beta-D-Glucopyranosyl fluoride tetraacetate is toxic and should be handled with care. It is corrosive and can cause skin and eye irritation. It should not be ingested or inhaled, and it should be used in a well-ventilated area. Safety protocols should be followed in all scientific experiments involving the compound.

Applications in Scientific Experiments:

Beta-D-Glucopyranosyl fluoride tetraacetate has several applications in scientific research. It is commonly used in glycosylation reactions to form glycosidic bonds. It can also be used for the synthesis of glycoproteins and the development of new drugs and treatments.

Current State of Research:

Beta-D-Glucopyranosyl fluoride tetraacetate is an active area of research in various fields, including medicinal chemistry, biochemistry, and organic chemistry. Researchers are looking for new ways to synthesize the compound and explore its potential applications in different fields.

Potential Implications in Various Fields of Research and Industry:

Beta-D-Glucopyranosyl fluoride tetraacetate has potential implications in various fields of research and industry. It can be used to synthesize new drugs and treatments for various diseases, including cancer and viral infections. It can also be used in the development of new materials, such as biodegradable plastics.

Limitations and Future Directions:

Despite its many uses, Beta-D-Glucopyranosyl fluoride tetraacetate has its limitations. It is toxic and needs to be handled with care. Researchers need to explore new ways to synthesize the compound and improve its yields. Future research should also focus on exploring the potential applications of the compound in different fields and industries.

Future Directions:

1. Developing new synthesis methods to increase yields and reduce costs.

2. Exploring the potential of Beta-D-Glucopyranosyl fluoride tetraacetate in drug discovery and development.

3. Studying the compound's potential applications in the development of new materials, such as biodegradable plastics.

4. Investigating the antiviral properties of the compound and its potential use in fighting viral infections.

5. Developing new analytical methods to study the properties and behavior of the compound.

6. Studying the structure-activity relationships of Beta-D-Glucopyranosyl fluoride tetraacetate to develop more potent and selective drugs.

7. Investigating the compound's potential applications in glycoprotein synthesis and modification.

8. Exploring the biological fate and disposition of Beta-D-Glucopyranosyl fluoride tetraacetate in living organisms.

9. Developing new chemical modifications of the compound to improve its physicochemical properties and biological activity.

10. Studying the compound's potential applications in gene therapy and immunotherapy.

CAS Number2823-46-3
Product Namebeta-D-Glucopyranosyl fluoride tetraacetate
IUPAC Name[(2R,3R,4S,5R,6S)-3,4,5-triacetyloxy-6-fluorooxan-2-yl]methyl acetate
Molecular FormulaC14H19FO9
Molecular Weight350.29 g/mol
InChIInChI=1S/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
InChI KeyJJXATNWYELAACC-RKQHYHRCSA-N
SMILESCC(=O)OCC1C(C(C(C(O1)F)OC(=O)C)OC(=O)C)OC(=O)C
Canonical SMILESCC(=O)OCC1C(C(C(C(O1)F)OC(=O)C)OC(=O)C)OC(=O)C
Isomeric SMILESCC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)F)OC(=O)C)OC(=O)C)OC(=O)C


CAS No: 2823-46-3 MDL No: MFCD01862267 Chemical Formula: C14H19FO9 Molecular Weight: 350.29

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