(3S,4S,5R)-5-((benzoyloxy)methyl)-4-fluorotetrahydrofuran-2,3-diyl diacetate
95%
- Product Code: 82891
CAS:
159099-24-8
| Molecular Weight: | 340.30 g./mol | Molecular Formula: | C₁₆H₁₇FO₇ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28975247 | |
| Melting Point: | Boiling Point: | 422.9±45.0 °C(Predicted) | |
| Density: | 1.31±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, inert atmosphere |
Product Description:
This compound is primarily utilized in the pharmaceutical and biochemical research fields. It serves as a key intermediate in the synthesis of nucleoside analogs, which are crucial for developing antiviral and anticancer drugs. Its structural features, including the fluorinated tetrahydrofuran ring, make it valuable for modifying the biological activity and stability of nucleoside-based therapeutics. Researchers also employ it in studies aimed at understanding the mechanisms of enzyme inhibition and drug resistance, particularly in viruses and cancer cells. Additionally, its benzoyl and acetyl protecting groups facilitate selective chemical transformations during complex molecule synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿14,724.00 |
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| 0.250 | 10-20 days | ฿24,543.00 |
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| 1.000 | 10-20 days | ฿38,241.00 |
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(3S,4S,5R)-5-((benzoyloxy)methyl)-4-fluorotetrahydrofuran-2,3-diyl diacetate
This compound is primarily utilized in the pharmaceutical and biochemical research fields. It serves as a key intermediate in the synthesis of nucleoside analogs, which are crucial for developing antiviral and anticancer drugs. Its structural features, including the fluorinated tetrahydrofuran ring, make it valuable for modifying the biological activity and stability of nucleoside-based therapeutics. Researchers also employ it in studies aimed at understanding the mechanisms of enzyme inhibition and drug resistance, particularly in viruses and cancer cells. Additionally, its benzoyl and acetyl protecting groups facilitate selective chemical transformations during complex molecule synthesis.
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