2-Acetamido-4-fluoro-1,3,6-tri-O-acetyl-2,4-dideoxy-D-glucopyranose
≥98%
- Product Code: 103685
CAS:
116049-57-1
| Molecular Weight: | 349.31 g./mol | Molecular Formula: | C₁₄H₂₀FNO₈ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | 1.30 g/cm3(Predicted) | Storage Condition: | -20°C |
Product Description:
This chemical is primarily utilized in the synthesis of modified sugars and glycosides, which are crucial in the development of pharmaceuticals and biochemical research. It serves as an intermediate in the production of nucleoside analogs, which are important in antiviral and anticancer drug development. The compound's unique structure allows for the introduction of fluorine atoms into sugar molecules, enhancing their biological activity and stability. Additionally, it is used in glycosylation reactions to study enzyme mechanisms and to create novel glycoconjugates for therapeutic and diagnostic applications. Its role in advancing carbohydrate chemistry makes it valuable in both academic and industrial settings.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Off-white Solid To Semi-solid |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿26,980.00 |
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| 0.010 | 10-20 days | ฿40,230.00 |
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2-Acetamido-4-fluoro-1,3,6-tri-O-acetyl-2,4-dideoxy-D-glucopyranose
This chemical is primarily utilized in the synthesis of modified sugars and glycosides, which are crucial in the development of pharmaceuticals and biochemical research. It serves as an intermediate in the production of nucleoside analogs, which are important in antiviral and anticancer drug development. The compound's unique structure allows for the introduction of fluorine atoms into sugar molecules, enhancing their biological activity and stability. Additionally, it is used in glycosylation reactions to study enzyme mechanisms and to create novel glycoconjugates for therapeutic and diagnostic applications. Its role in advancing carbohydrate chemistry makes it valuable in both academic and industrial settings.
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