(4-(2-((tert-Butoxycarbonyl)(cyclohexyl)amino) ethoxy)-3-fluorophenyl)boronic acid
98%
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This chemical is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry. It serves as a key intermediate in the development of pharmaceutical compounds, especially those targeting enzyme inhibition or receptor modulation. The boronic acid group enables its use in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This makes it valuable in constructing complex molecules for drug discovery. Additionally, the presence of the tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthetic processes, enhancing its versatility in synthesizing biologically active molecules. Its application extends to the preparation of potential therapeutics for diseases such as cancer, inflammation, and metabolic disorders.
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