1,3,5-Tri-O-benzoyl-2-deoxy-2-fluoro-alpha-L-arabinofuranose
98%
- Product Code: 103814
CAS:
171721-00-9
| Molecular Weight: | 464.44 g./mol | Molecular Formula: | C₂₆H₂₁FO₇ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily used in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. It serves as a key intermediate in the modification of sugar moieties, enabling the creation of compounds with enhanced biological activity and specificity. Its fluorinated structure is particularly valuable in medicinal chemistry, as it can improve the metabolic stability and binding affinity of the resulting molecules. Researchers utilize it to explore new therapeutic agents, especially in the field of antiviral research, where modified nucleosides play a significant role in inhibiting viral replication. Additionally, its benzoyl groups provide protection during synthetic processes, ensuring precise and controlled reactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,106.00 |
+
-
|
| 5.000 | 10-20 days | ฿8,073.00 |
+
-
|
| 10.000 | 10-20 days | ฿14,391.00 |
+
-
|
1,3,5-Tri-O-benzoyl-2-deoxy-2-fluoro-alpha-L-arabinofuranose
This chemical is primarily used in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. It serves as a key intermediate in the modification of sugar moieties, enabling the creation of compounds with enhanced biological activity and specificity. Its fluorinated structure is particularly valuable in medicinal chemistry, as it can improve the metabolic stability and binding affinity of the resulting molecules. Researchers utilize it to explore new therapeutic agents, especially in the field of antiviral research, where modified nucleosides play a significant role in inhibiting viral replication. Additionally, its benzoyl groups provide protection during synthetic processes, ensuring precise and controlled reactions.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
฿0.00
฿0.00
Total :