(5-Bromo-2-fluoro-3-methylphenyl)boronic acid
98%
- Product Code: 79571
CAS:
957120-61-5
| Molecular Weight: | 232.84 g./mol | Molecular Formula: | C₇H₇BBrFO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09800868 | |
| Melting Point: | Boiling Point: | 345.8°C at 760 mmHg | |
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the construction of complex organic molecules, especially in the pharmaceutical and materials science industries. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common motifs in drug discovery and development. Additionally, it is employed in the synthesis of advanced materials, such as organic semiconductors and liquid crystals, due to its ability to introduce specific functional groups into aromatic systems. Its fluorine and bromine substituents further enhance its reactivity and selectivity in various chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿468.00 |
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| 1.000 | 10-20 days | ฿882.00 |
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| 5.000 | 10-20 days | ฿2,709.00 |
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| 10.000 | 10-20 days | ฿4,662.00 |
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(5-Bromo-2-fluoro-3-methylphenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the construction of complex organic molecules, especially in the pharmaceutical and materials science industries. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common motifs in drug discovery and development. Additionally, it is employed in the synthesis of advanced materials, such as organic semiconductors and liquid crystals, due to its ability to introduce specific functional groups into aromatic systems. Its fluorine and bromine substituents further enhance its reactivity and selectivity in various chemical transformations.
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