(3-Fluoro-5-((4-methoxybenzyl)carbamoyl)phenyl)boronic acid
98%
- Product Code: 89121
CAS:
1704082-30-3
| Molecular Weight: | 303.1 g./mol | Molecular Formula: | C₁₅H₁₅BFNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20040277 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables it to form stable covalent bonds with various organic molecules, making it valuable for constructing complex chemical structures. It is often employed in the development of pharmaceuticals, where it aids in the creation of biologically active compounds. Additionally, it finds use in materials science for designing advanced polymers and functional materials. Its specific structure, including the fluoro and methoxybenzyl groups, allows for precise tuning of reactivity and selectivity in synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | ฿33,410.00 |
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(3-Fluoro-5-((4-methoxybenzyl)carbamoyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables it to form stable covalent bonds with various organic molecules, making it valuable for constructing complex chemical structures. It is often employed in the development of pharmaceuticals, where it aids in the creation of biologically active compounds. Additionally, it finds use in materials science for designing advanced polymers and functional materials. Its specific structure, including the fluoro and methoxybenzyl groups, allows for precise tuning of reactivity and selectivity in synthetic processes.
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