Boronic acid,B-(2-bromo-6-fluoro-3-methoxyphenyl)-
98%
- Product Code: 89811
CAS:
957062-89-4
| Molecular Weight: | 248.84 g./mol | Molecular Formula: | C₇H₇BBrFO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08276828 | |
| Melting Point: | 130-135℃ | Boiling Point: | |
| Density: | Storage Condition: | Dry, sealed, 2-8℃ |
Product Description:
Used extensively in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a crucial building block for constructing complex molecules. Its boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The presence of bromo and fluoro substituents enhances its reactivity and selectivity in coupling reactions, making it valuable for creating biologically active compounds. Additionally, its methoxy group can influence the electronic properties of the resulting molecules, aiding in the development of drugs targeting specific biological pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿675.00 |
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| 5.000 | 10-20 days | ฿1,728.00 |
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Boronic acid,B-(2-bromo-6-fluoro-3-methoxyphenyl)-
Used extensively in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a crucial building block for constructing complex molecules. Its boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The presence of bromo and fluoro substituents enhances its reactivity and selectivity in coupling reactions, making it valuable for creating biologically active compounds. Additionally, its methoxy group can influence the electronic properties of the resulting molecules, aiding in the development of drugs targeting specific biological pathways.
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