3-Fluoro-5-(diethylcarbamoyl)phenylboronic acid
98%
- Product Code: 90168
CAS:
871332-64-8
| Molecular Weight: | 239.05 g./mol | Molecular Formula: | C₁₁H₁₅BFNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07363794 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used in organic synthesis as a key intermediate for the development of pharmaceuticals, particularly in the creation of enzyme inhibitors and receptor modulators. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, making it valuable for constructing complex molecules in drug discovery. Additionally, it is employed in the preparation of bioactive compounds targeting neurological disorders due to its unique structural properties. The fluorine atom enhances metabolic stability and binding affinity, making it a preferred choice in medicinal chemistry research.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | white solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $377.53 |
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| 0.500 | 10-20 days | $943.82 |
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3-Fluoro-5-(diethylcarbamoyl)phenylboronic acid
Used in organic synthesis as a key intermediate for the development of pharmaceuticals, particularly in the creation of enzyme inhibitors and receptor modulators. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, making it valuable for constructing complex molecules in drug discovery. Additionally, it is employed in the preparation of bioactive compounds targeting neurological disorders due to its unique structural properties. The fluorine atom enhances metabolic stability and binding affinity, making it a preferred choice in medicinal chemistry research.
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