4-Fluoro-3-methylpyridine-5-boronic acid
95%
- Product Code: 92181
CAS:
2225155-44-0
| Molecular Weight: | 154.9346832 g./mol | Molecular Formula: | C₆H₇BFNO₂ |
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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 the Suzuki-Miyaura reaction. It serves as a key building block for the introduction of the 4-fluoro-3-methylpyridine moiety into more complex molecules. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of biologically active compounds, where the fluorine atom can enhance metabolic stability and binding affinity. Its applications also extend to the creation of ligands for catalysis and the modification of organic frameworks for specialized industrial uses.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.005 | 10-20 days | $413.71 |
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| 0.025 | 10-20 days | $1,772.03 |
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| 0.100 | 10-20 days | $5,316.88 |
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4-Fluoro-3-methylpyridine-5-boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the introduction of the 4-fluoro-3-methylpyridine moiety into more complex molecules. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of biologically active compounds, where the fluorine atom can enhance metabolic stability and binding affinity. Its applications also extend to the creation of ligands for catalysis and the modification of organic frameworks for specialized industrial uses.
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