N-Phenyl 4-borono-2-fluorobenzamide
95%
- Product Code: 121571
CAS:
874288-40-1
| Molecular Weight: | 259.04 g./mol | Molecular Formula: | C₁₃H₁₁BFNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08436025 | |
| Melting Point: | 219-221 °C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used primarily in the field of medicinal chemistry, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to create complex organic compounds, including pharmaceuticals. The fluorine atom enhances its potential in drug development by improving metabolic stability and binding affinity. It is particularly relevant in the design of protease inhibitors and other therapeutic agents targeting specific enzymes or receptors. Additionally, its structural features make it a candidate for research in cancer therapy and inflammatory diseases.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿8,991.00 |
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| 1.000 | 10-20 days | ฿31,671.00 |
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N-Phenyl 4-borono-2-fluorobenzamide
Used primarily in the field of medicinal chemistry, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to create complex organic compounds, including pharmaceuticals. The fluorine atom enhances its potential in drug development by improving metabolic stability and binding affinity. It is particularly relevant in the design of protease inhibitors and other therapeutic agents targeting specific enzymes or receptors. Additionally, its structural features make it a candidate for research in cancer therapy and inflammatory diseases.
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