(2-(bis(ethyl-d5)amino)pyrimidin-5-yl)boronic acid
95%
- Product Code: 56320
CAS:
2241877-02-9
| Molecular Weight: | 205.08827778 g./mol | Molecular Formula: | C₈H₄BD₁₀N₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of complex molecules. It serves as a key intermediate in the creation of targeted therapies, especially in the development of kinase inhibitors. These inhibitors play a crucial role in treating various cancers by blocking specific enzymes that promote tumor growth. Additionally, its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method in organic chemistry to form carbon-carbon bonds. This reaction is essential for constructing biologically active compounds and advanced materials. The deuterium-labeled ethyl groups in the compound enhance its utility in metabolic studies, allowing researchers to track and analyze drug behavior in biological systems with greater precision.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿269,620.00 |
+
-
|
| 0.025 | 10-20 days | ฿720,000.00 |
+
-
|
(2-(bis(ethyl-d5)amino)pyrimidin-5-yl)boronic acid
This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of complex molecules. It serves as a key intermediate in the creation of targeted therapies, especially in the development of kinase inhibitors. These inhibitors play a crucial role in treating various cancers by blocking specific enzymes that promote tumor growth. Additionally, its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method in organic chemistry to form carbon-carbon bonds. This reaction is essential for constructing biologically active compounds and advanced materials. The deuterium-labeled ethyl groups in the compound enhance its utility in metabolic studies, allowing researchers to track and analyze drug behavior in biological systems with greater precision.
| 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 :