Potassium N-cyclohexyl-aminomethyltrifluoroborate is a specialized organotrifluoroborate salt utilized as a stable and efficient reagent in organic synthesis, particularly for Suzuki-Miyaura cross-coupling reactions. It functions as a boron nucleophile, facilitating the selective transfer of the N-cyclohexyl-aminomethyl group to aryl or vinyl halides, thereby forming carbon-nitrogen and carbon-carbon bonds in complex molecules. This reagent's trifluoroborate moiety provides superior stability, reactivity, and selectivity compared to traditional boronic acids, making it ideal for pharmaceutical and agrochemical applications where precise control is essential. It is also employed in the synthesis of advanced materials, including polymers and liquid crystals, enabling the construction of intricate molecular architectures.