Pyridine-4-Boronic Acid Hydrochloride
≥98%
- Product Code: 91183
CAS:
913835-65-1
| Molecular Weight: | 159.38 g./mol | Molecular Formula: | C₅H₇BNO₂Cl |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
Pyridine-4-Boronic Acid Hydrochloride is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the coupling of aryl or vinyl halides with arylboronic acids to create complex organic molecules.
In medicinal chemistry, it serves as a building block for designing and synthesizing drug candidates, especially in the development of kinase inhibitors and other bioactive compounds. Its pyridine moiety contributes to the molecule's ability to interact with biological targets, enhancing its utility in drug discovery.
Additionally, it finds applications in material science, where it is used to modify surfaces or create functionalized polymers. Its ability to form stable covalent bonds makes it suitable for developing sensors, catalysts, and other advanced materials. Overall, its versatility and reactivity make it a crucial component in various chemical and industrial processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿333.00 |
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| 5.000 | 10-20 days | ฿1,071.00 |
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| 25.000 | 10-20 days | ฿3,744.00 |
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Pyridine-4-Boronic Acid Hydrochloride
Pyridine-4-Boronic Acid Hydrochloride is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the coupling of aryl or vinyl halides with arylboronic acids to create complex organic molecules.
In medicinal chemistry, it serves as a building block for designing and synthesizing drug candidates, especially in the development of kinase inhibitors and other bioactive compounds. Its pyridine moiety contributes to the molecule's ability to interact with biological targets, enhancing its utility in drug discovery.
Additionally, it finds applications in material science, where it is used to modify surfaces or create functionalized polymers. Its ability to form stable covalent bonds makes it suitable for developing sensors, catalysts, and other advanced materials. Overall, its versatility and reactivity make it a crucial component in various chemical and industrial processes.
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