4-Fluoro-2-bromopyridine-5-boronic acid
95%
- Product Code: 92176
CAS:
2225171-58-2
| Molecular Weight: | 219.8041632 g./mol | Molecular Formula: | C₅H₄BBrFNO₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
4-Fluoro-2-bromopyridine-5-boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. This reaction is widely employed to form carbon-carbon bonds, making the compound valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key functional group for coupling with aryl or vinyl halides, while the fluorine and bromine substituents enhance its reactivity and selectivity. Additionally, it serves as a building block in the development of complex molecules, especially in medicinal chemistry for drug discovery and development. Its unique structure allows for precise modifications, making it a versatile intermediate in synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | €277.54 |
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| 0.025 | 10-20 days | €1,188.77 |
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| 0.100 | 10-20 days | €3,566.85 |
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4-Fluoro-2-bromopyridine-5-boronic acid
4-Fluoro-2-bromopyridine-5-boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. This reaction is widely employed to form carbon-carbon bonds, making the compound valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key functional group for coupling with aryl or vinyl halides, while the fluorine and bromine substituents enhance its reactivity and selectivity. Additionally, it serves as a building block in the development of complex molecules, especially in medicinal chemistry for drug discovery and development. Its unique structure allows for precise modifications, making it a versatile intermediate in synthetic chemistry.
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