3-Fluoro-4-(2-(4-oxopiperidin-1-yl)ethoxy)phenylboronic acid
98%
science Other reagents with same CAS 1704064-10-7
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description Product Description
This compound is primarily utilized in organic synthesis and medicinal chemistry as a key intermediate in the development of biologically active molecules. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The presence of the fluorine atom enhances its potential in drug design, as fluorine is often incorporated to improve metabolic stability and binding affinity. Additionally, the piperidinone moiety contributes to its application in the creation of compounds targeting neurological and metabolic disorders, as this structural feature is commonly found in molecules with therapeutic potential. Its unique structure also makes it a candidate for research in enzyme inhibition and receptor modulation studies.
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