(2-Bromo-3-fluorophenyl)boronic acid
98%
- Product Code: 43177
CAS:
731817-89-3
| Molecular Weight: | 218.82 g./mol | Molecular Formula: | C₆H₅BBrFO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27996941 | |
| Melting Point: | Boiling Point: | 328.6±52.0 °C | |
| Density: | 1.75±0.1 g/cm3 | Storage Condition: | 2-8°C, inert atmosphere |
Product Description:
(2-Bromo-3-fluorophenyl)boronic acid is primarily utilized in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry to construct biaryl compounds, which are essential in the development of various drugs and bioactive molecules. The presence of both bromo and fluoro substituents on the phenyl ring enhances its reactivity and selectivity in coupling processes, making it valuable for creating complex organic structures. Additionally, it is used in material science for the synthesis of advanced polymers and organic electronic materials, where precise molecular design is crucial. Its role in catalysis and as a building block in medicinal chemistry underscores its importance in research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿16,335.00 |
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| 1.000 | 10-20 days | ฿38,016.00 |
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(2-Bromo-3-fluorophenyl)boronic acid
(2-Bromo-3-fluorophenyl)boronic acid is primarily utilized in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry to construct biaryl compounds, which are essential in the development of various drugs and bioactive molecules. The presence of both bromo and fluoro substituents on the phenyl ring enhances its reactivity and selectivity in coupling processes, making it valuable for creating complex organic structures. Additionally, it is used in material science for the synthesis of advanced polymers and organic electronic materials, where precise molecular design is crucial. Its role in catalysis and as a building block in medicinal chemistry underscores its importance in research and industrial applications.
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