(3-(Cyclohexylcarbamoyl)-5-nitrophenyl)boronic acid
97%
science Other reagents with same CAS 871332-85-3
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Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl compounds with nitro and amide functional groups. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research. The presence of a cyclohexylcarbamoyl group enhances solubility and influences molecular conformation, which can be beneficial in drug design. Commonly employed in the development of bioactive molecules and functional materials requiring specific electronic or steric properties.
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