((2R,3R)-3-(Benzoyloxy)-4,4-difluoro-5-hydroxytetrahydrofuran-2-yl)methyl benzoate
95%
- Product Code: 123567
CAS:
1173824-58-2
| Molecular Weight: | 378.32 g./mol | Molecular Formula: | C₁₉H₁₆F₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08703624 | |
| Melting Point: | Boiling Point: | 495.9±45.0 °C(Predicted) | |
| Density: | 1.41 g/cm3 | Storage Condition: | 2-8°C, inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of nucleoside analogs. These analogs are crucial in the development of antiviral and anticancer drugs, as they can mimic natural nucleosides and interfere with viral replication or cancer cell proliferation. Its structure, featuring a difluoro and benzoyl group, enhances its ability to act as a building block for modified nucleosides, which are often designed to improve drug stability and efficacy. Additionally, it may be used in research to study enzyme interactions and mechanisms of action in biochemical pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,318.00 |
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| 0.250 | 10-20 days | ฿10,737.00 |
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| 1.000 | 10-20 days | ฿28,980.00 |
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((2R,3R)-3-(Benzoyloxy)-4,4-difluoro-5-hydroxytetrahydrofuran-2-yl)methyl benzoate
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of nucleoside analogs. These analogs are crucial in the development of antiviral and anticancer drugs, as they can mimic natural nucleosides and interfere with viral replication or cancer cell proliferation. Its structure, featuring a difluoro and benzoyl group, enhances its ability to act as a building block for modified nucleosides, which are often designed to improve drug stability and efficacy. Additionally, it may be used in research to study enzyme interactions and mechanisms of action in biochemical pathways.
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