(2-Bromo-6-fluorophenyl)boronic acid
97%
- Product Code: 89812
CAS:
913835-80-0
| Molecular Weight: | 218.82 g./mol | Molecular Formula: | C₆H₅BBrFO₂ |
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| EC Number: | MDL Number: | MFCD05664309 | |
| Melting Point: | 138-143°C | Boiling Point: | 324.4°C |
| Density: | Storage Condition: | 2-8°C |
Product Description:
(2-Bromo-6-fluorophenyl)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, including pharmaceuticals, agrochemicals, and advanced materials. Its unique structure, featuring both bromo and fluoro substituents, allows for selective functionalization, making it valuable in designing compounds with specific properties. Additionally, it serves as a key intermediate in the development of bioactive molecules, contributing to drug discovery and medicinal chemistry research. Its stability and reactivity also make it a useful reagent in the synthesis of heterocycles and other aromatic compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 1.000 | 10-20 days | £9.57 |
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| 5.000 | 10-20 days | £19.54 |
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(2-Bromo-6-fluorophenyl)boronic acid
(2-Bromo-6-fluorophenyl)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, including pharmaceuticals, agrochemicals, and advanced materials. Its unique structure, featuring both bromo and fluoro substituents, allows for selective functionalization, making it valuable in designing compounds with specific properties. Additionally, it serves as a key intermediate in the development of bioactive molecules, contributing to drug discovery and medicinal chemistry research. Its stability and reactivity also make it a useful reagent in the synthesis of heterocycles and other aromatic compounds.
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