1-benzyl-3-[2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea
95%
- Product Code: 80026
CAS:
2246759-61-3
| Molecular Weight: | 370.2256 g./mol | Molecular Formula: | C₂₀H₂₄BFN₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD32206428 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly as an intermediate in the synthesis of biologically active molecules. Its structure, featuring a urea moiety and a boronate ester group, makes it valuable in the design of protease inhibitors and other therapeutic agents targeting specific enzymes or proteins. The boronate ester functionality is often leveraged in Suzuki-Miyaura cross-coupling reactions, a key method in constructing complex organic molecules for pharmaceutical applications. Additionally, its fluorine substituent can enhance metabolic stability and binding affinity, making it a useful component in the development of drugs for conditions such as cancer, inflammation, and infectious diseases. Researchers also explore its potential in creating PET (positron emission tomography) imaging agents due to the fluorine atom’s role in radiolabeling. Overall, this compound serves as a versatile building block in the synthesis of innovative drug candidates and diagnostic tools.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿4,896.00 |
+
-
|
| 0.250 | 10-20 days | ฿15,300.00 |
+
-
|
1-benzyl-3-[2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea
This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly as an intermediate in the synthesis of biologically active molecules. Its structure, featuring a urea moiety and a boronate ester group, makes it valuable in the design of protease inhibitors and other therapeutic agents targeting specific enzymes or proteins. The boronate ester functionality is often leveraged in Suzuki-Miyaura cross-coupling reactions, a key method in constructing complex organic molecules for pharmaceutical applications. Additionally, its fluorine substituent can enhance metabolic stability and binding affinity, making it a useful component in the development of drugs for conditions such as cancer, inflammation, and infectious diseases. Researchers also explore its potential in creating PET (positron emission tomography) imaging agents due to the fluorine atom’s role in radiolabeling. Overall, this compound serves as a versatile building block in the synthesis of innovative drug candidates and diagnostic tools.
| 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 :