2-Fluoro-6-(piperidin-3-yl)pyridine-4-boronic acid
95%
- Product Code: 91664
CAS:
2225152-72-5
| Molecular Weight: | 224.0397632 g./mol | Molecular Formula: | C₁₀H₁₄BFN₂O₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the piperidine ring and fluorine atom enhances its reactivity and selectivity, allowing for the creation of diverse chemical structures. It is often employed in the development of drug candidates, where its unique structure contributes to the optimization of biological activity and pharmacokinetic properties. Additionally, it serves as a building block in materials science for the design of advanced polymers and functional materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿56,720.00 |
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| 0.025 | 10-20 days | ฿148,880.00 |
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2-Fluoro-6-(piperidin-3-yl)pyridine-4-boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the piperidine ring and fluorine atom enhances its reactivity and selectivity, allowing for the creation of diverse chemical structures. It is often employed in the development of drug candidates, where its unique structure contributes to the optimization of biological activity and pharmacokinetic properties. Additionally, it serves as a building block in materials science for the design of advanced polymers and functional materials.
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