4-Fluoro-2-(3-methyl-1H-pyrazol-1-yl)pyridine-5-boronic acid
95%
- Product Code: 92142
CAS:
2225175-45-9
| Molecular Weight: | 220.9960632 g./mol | Molecular Formula: | C₉H₉BFN₃O₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
This chemical is primarily used in the field of organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of complex organic compounds, especially in the pharmaceutical industry. Its boronic acid group makes it highly valuable in Suzuki-Miyaura coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of drugs, agrochemicals, and advanced materials. Additionally, its pyrazole and pyridine moieties contribute to its utility in designing molecules with potential biological activity, such as enzyme inhibitors or receptor modulators. Its applications extend to the development of new therapeutic agents and functional materials due to its structural versatility.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿10,520.00 |
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| 0.025 | 10-20 days | ฿45,060.00 |
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| 0.100 | 10-20 days | ฿135,200.00 |
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4-Fluoro-2-(3-methyl-1H-pyrazol-1-yl)pyridine-5-boronic acid
This chemical is primarily used in the field of organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of complex organic compounds, especially in the pharmaceutical industry. Its boronic acid group makes it highly valuable in Suzuki-Miyaura coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of drugs, agrochemicals, and advanced materials. Additionally, its pyrazole and pyridine moieties contribute to its utility in designing molecules with potential biological activity, such as enzyme inhibitors or receptor modulators. Its applications extend to the development of new therapeutic agents and functional materials due to its structural versatility.
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