2-Fluoro-6-(tert-butyl)pyridine-4-boronic acid
95%
- Product Code: 91665
CAS:
2225175-67-5
| Molecular Weight: | 197.0144232 g./mol | Molecular Formula: | C₉H₁₃BFNO₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a versatile building block for the introduction of the 2-fluoro-6-(tert-butyl)pyridine moiety into more complex molecules. Its boronic acid group enables efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and materials science. Additionally, the tert-butyl group enhances steric stability, which can be advantageous in designing compounds with specific structural or functional properties. Its applications are often seen in the synthesis of biologically active compounds, where the fluorinated pyridine structure can improve metabolic stability and binding affinity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿47,800.00 |
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| 0.025 | 10-20 days | ฿133,300.00 |
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2-Fluoro-6-(tert-butyl)pyridine-4-boronic acid
This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a versatile building block for the introduction of the 2-fluoro-6-(tert-butyl)pyridine moiety into more complex molecules. Its boronic acid group enables efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and materials science. Additionally, the tert-butyl group enhances steric stability, which can be advantageous in designing compounds with specific structural or functional properties. Its applications are often seen in the synthesis of biologically active compounds, where the fluorinated pyridine structure can improve metabolic stability and binding affinity.
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