(6-Bromo-2-fluoropyridin-3-yl)boronic acid
98%
- Product Code: 91374
CAS:
910649-58-0
| Molecular Weight: | 219.81 g./mol | Molecular Formula: | C₅H₄BBrFNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11045051 | |
| Melting Point: | Boiling Point: | 364.654℃at 760 mmHg | |
| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
(6-Bromo-2-fluoropyridin-3-yl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in the development of biologically active compounds. Additionally, it is utilized in the synthesis of heterocyclic compounds, which are crucial in drug discovery and material science. The bromo and fluoro substituents on the pyridine ring enhance its reactivity and selectivity in various chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.025 | 10-20 days | $24.84 |
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| 0.100 | 10-20 days | $34.83 |
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| 0.250 | 10-20 days | $44.01 |
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| 1.000 | 10-20 days | $118.27 |
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| 5.000 | 10-20 days | $413.41 |
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(6-Bromo-2-fluoropyridin-3-yl)boronic acid
(6-Bromo-2-fluoropyridin-3-yl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in the development of biologically active compounds. Additionally, it is utilized in the synthesis of heterocyclic compounds, which are crucial in drug discovery and material science. The bromo and fluoro substituents on the pyridine ring enhance its reactivity and selectivity in various chemical transformations.
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