3-Fluoro-5-(4-methyl-1H-pyrazol-1-yl)phenylboronic acid
95%
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This chemical, featuring a fluoro substituent and a 4-methyl-1H-pyrazol-1-yl group on the phenyl ring, is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for the creation of complex biaryl compounds, which are essential in the development of pharmaceuticals and agrochemicals. The boronic acid group facilitates the formation of carbon-carbon bonds, while the pyrazole and fluorine functionalities enhance reaction efficiency and specificity, enabling the synthesis of diverse organic molecules. Additionally, it is employed in the preparation of advanced materials and in the study of molecular interactions due to its unique structural properties. Its applications extend to research in medicinal chemistry, where it aids in the design and synthesis of potential drug candidates targeting various diseases, owing to its modifiable structure and biocompatibility.
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