2-Fluoro-6-(tert-butyl)pyridine-3-boronic acid
95%
- Product Code: 91670
CAS:
2225177-12-6
| Molecular Weight: | 197.0144232 g./mol | Molecular Formula: | C₉H₁₃BFNO₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
2-Fluoro-6-(tert-butyl)pyridine-3-boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry to create complex molecules for drug development. The compound’s boronic acid group acts as a key functional group, enabling the formation of carbon-carbon bonds, which are essential for constructing active pharmaceutical ingredients (APIs). Its fluorine and tert-butyl substituents enhance its reactivity and selectivity, making it a valuable intermediate in the synthesis of biologically active compounds. Additionally, it is utilized in material science for the development of organic electronic materials and polymers.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿10,520.00 |
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| 0.025 | 10-20 days | ฿45,060.00 |
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| 0.100 | 10-20 days | ฿135,200.00 |
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2-Fluoro-6-(tert-butyl)pyridine-3-boronic acid
2-Fluoro-6-(tert-butyl)pyridine-3-boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry to create complex molecules for drug development. The compound’s boronic acid group acts as a key functional group, enabling the formation of carbon-carbon bonds, which are essential for constructing active pharmaceutical ingredients (APIs). Its fluorine and tert-butyl substituents enhance its reactivity and selectivity, making it a valuable intermediate in the synthesis of biologically active compounds. Additionally, it is utilized in material science for the development of organic electronic materials and polymers.
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