(2R,3R,4S,5R)-2-(acetoxymethyl)-6-fluorotetrahydro-2H-pyran-3,4,5-triyl triacetate
95%
- Product Code: 82856
CAS:
162489-61-4
| Molecular Weight: | 350.29 g./mol | Molecular Formula: | C₁₄H₁₉FO₉ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 374.8±42.0 °C(Predicted) | |
| Density: | 1.30±0.1 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer medications. Its structure allows it to act as a precursor in the modification of nucleosides, enhancing their therapeutic potential. Specifically, it is used to introduce fluorine atoms into the sugar moiety of nucleosides, improving their stability and bioavailability. This modification is particularly valuable in creating drugs that target viral replication enzymes or cancer cell proliferation. Additionally, its acetylated groups facilitate selective deprotection during synthetic processes, enabling precise chemical transformations. This compound plays a significant role in medicinal chemistry, contributing to the design of more effective and targeted therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,552.00 |
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| 0.250 | 10-20 days | ฿12,285.00 |
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| 1.000 | 10-20 days | ฿24,921.00 |
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(2R,3R,4S,5R)-2-(acetoxymethyl)-6-fluorotetrahydro-2H-pyran-3,4,5-triyl triacetate
This compound is primarily utilized in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer medications. Its structure allows it to act as a precursor in the modification of nucleosides, enhancing their therapeutic potential. Specifically, it is used to introduce fluorine atoms into the sugar moiety of nucleosides, improving their stability and bioavailability. This modification is particularly valuable in creating drugs that target viral replication enzymes or cancer cell proliferation. Additionally, its acetylated groups facilitate selective deprotection during synthetic processes, enabling precise chemical transformations. This compound plays a significant role in medicinal chemistry, contributing to the design of more effective and targeted therapeutic agents.
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