2-(Piperidin-1-yl)pyridin-4-ylboronic acid
95%
- Product Code: 56368
CAS:
1256358-82-3
| Molecular Weight: | 206.0493 g./mol | Molecular Formula: | C₁₀H₁₅BN₂O₂ |
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| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
2-(Piperidin-1-yl)pyridin-4-ylboronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry to create complex molecules by forming carbon-carbon bonds, which are essential in drug development. The boronic acid group in the compound acts as a key functional group, enabling the coupling with aryl or vinyl halides to produce biaryl or styrene derivatives. These derivatives are often intermediates in the synthesis of active pharmaceutical ingredients (APIs) and other biologically active compounds. Additionally, its piperidine moiety can contribute to the biological activity of the final product, making it valuable in medicinal chemistry. The compound is also utilized in material science for the development of organic electronic materials and polymers. Its stability and reactivity make it a versatile reagent in both academic research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿8,982.00 |
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| 0.025 | 10-20 days | ฿29,700.00 |
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| 0.100 | 10-20 days | ฿82,800.00 |
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2-(Piperidin-1-yl)pyridin-4-ylboronic acid
2-(Piperidin-1-yl)pyridin-4-ylboronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry to create complex molecules by forming carbon-carbon bonds, which are essential in drug development. The boronic acid group in the compound acts as a key functional group, enabling the coupling with aryl or vinyl halides to produce biaryl or styrene derivatives. These derivatives are often intermediates in the synthesis of active pharmaceutical ingredients (APIs) and other biologically active compounds. Additionally, its piperidine moiety can contribute to the biological activity of the final product, making it valuable in medicinal chemistry. The compound is also utilized in material science for the development of organic electronic materials and polymers. Its stability and reactivity make it a versatile reagent in both academic research and industrial applications.
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