[4-[(2-fluorophenyl)carbamoyl]phenyl]boronic acid
98%
- Product Code: 89179
CAS:
874288-06-9
| Molecular Weight: | 259.04 g./mol | Molecular Formula: | C₁₃H₁₁BFNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09027205 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.34g/mL | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, where it acts as a key intermediate for forming carbon-carbon bonds. Its boronic acid group enables it to couple with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable for constructing complex organic molecules. Additionally, it is employed in the development of pharmaceuticals and agrochemicals, where its structure contributes to the synthesis of biologically active compounds. Its fluorophenyl group can enhance the stability and binding affinity of the resulting molecules, making it useful in drug discovery and material science applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿14,930.00 |
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[4-[(2-fluorophenyl)carbamoyl]phenyl]boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, where it acts as a key intermediate for forming carbon-carbon bonds. Its boronic acid group enables it to couple with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable for constructing complex organic molecules. Additionally, it is employed in the development of pharmaceuticals and agrochemicals, where its structure contributes to the synthesis of biologically active compounds. Its fluorophenyl group can enhance the stability and binding affinity of the resulting molecules, making it useful in drug discovery and material science applications.
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