(2'R)-2'-Deoxy-2'-fluoro-2'-methyluridine 3',5'-dibenzoate
95%
- Product Code: 82833
CAS:
863329-65-1
| Molecular Weight: | 468.43 g./mol | Molecular Formula: | C₂₄H₂₁FN₂O₇ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27918666 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of modified nucleosides, which are crucial for developing antiviral and anticancer drugs. The fluorine and methyl groups at the 2' position enhance the stability and bioavailability of the resulting nucleoside analogs, making them more effective in targeting viral replication or cancer cell proliferation. Additionally, the dibenzoate protection at the 3' and 5' positions allows for selective deprotection and further functionalization, enabling the creation of diverse therapeutic agents. Its application is particularly significant in the design of prodrugs and nucleotide analogs used in treatments for diseases like hepatitis C and certain types of cancer.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $324.03 |
+
-
|
(2'R)-2'-Deoxy-2'-fluoro-2'-methyluridine 3',5'-dibenzoate
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of modified nucleosides, which are crucial for developing antiviral and anticancer drugs. The fluorine and methyl groups at the 2' position enhance the stability and bioavailability of the resulting nucleoside analogs, making them more effective in targeting viral replication or cancer cell proliferation. Additionally, the dibenzoate protection at the 3' and 5' positions allows for selective deprotection and further functionalization, enabling the creation of diverse therapeutic agents. Its application is particularly significant in the design of prodrugs and nucleotide analogs used in treatments for diseases like hepatitis C and certain types of cancer.
| 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 :