4-Fluoro-3-bromopyridine-5-boronic acid
95%
- Product Code: 92180
CAS:
2225177-26-2
| Molecular Weight: | 219.8041632 g./mol | Molecular Formula: | C₅H₄BBrFNO₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
4-Fluoro-3-bromopyridine-5-boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. This reaction is essential for forming carbon-carbon bonds, which is crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. The compound’s boronic acid group acts as a key functional group, enabling it to couple with various aryl or vinyl halides, making it valuable in constructing complex organic molecules. Additionally, its fluorine and bromine substituents provide versatility in further chemical modifications, allowing for the creation of diverse derivatives with specific properties. Its applications are particularly significant in medicinal chemistry, where it aids in the synthesis of drug candidates and biologically active compounds.
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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4-Fluoro-3-bromopyridine-5-boronic acid
4-Fluoro-3-bromopyridine-5-boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. This reaction is essential for forming carbon-carbon bonds, which is crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. The compound’s boronic acid group acts as a key functional group, enabling it to couple with various aryl or vinyl halides, making it valuable in constructing complex organic molecules. Additionally, its fluorine and bromine substituents provide versatility in further chemical modifications, allowing for the creation of diverse derivatives with specific properties. Its applications are particularly significant in medicinal chemistry, where it aids in the synthesis of drug candidates and biologically active compounds.
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