4-Fluoro-2-(4-methyl-1H-pyrazol-1-yl)pyridine-5-boronic acid
95%
- Product Code: 92145
CAS:
2225169-40-2
| Molecular Weight: | 220.9960632 g./mol | Molecular Formula: | C₉H₉BFN₃O₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic acid group enables it to act as a key building block for creating complex organic molecules, often used in the development of pharmaceuticals and agrochemicals. The presence of the pyrazole and pyridine rings enhances its ability to interact with biological targets, making it valuable in drug discovery for designing compounds with potential therapeutic effects. Additionally, its fluorine substituent can influence the metabolic stability and binding affinity of the resulting molecules, further expanding its applications in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.005 | 10-20 days | £237.93 |
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| 0.025 | 10-20 days | £1,019.12 |
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| 0.100 | 10-20 days | £3,057.82 |
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4-Fluoro-2-(4-methyl-1H-pyrazol-1-yl)pyridine-5-boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic acid group enables it to act as a key building block for creating complex organic molecules, often used in the development of pharmaceuticals and agrochemicals. The presence of the pyrazole and pyridine rings enhances its ability to interact with biological targets, making it valuable in drug discovery for designing compounds with potential therapeutic effects. Additionally, its fluorine substituent can influence the metabolic stability and binding affinity of the resulting molecules, further expanding its applications in medicinal chemistry.
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