2-Trifluoromethyl-4-(4-methylimidazol-1-yl)phenylboronic acid
95%
science Other reagents with same CAS 2225178-35-6
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Used primarily in organic synthesis and pharmaceutical research, this compound serves as a key intermediate in the development of biologically active molecules. Its boronic acid group facilitates Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for constructing complex organic structures. Additionally, its trifluoromethyl and imidazole moieties enhance its utility in drug discovery, particularly in designing compounds with improved metabolic stability and binding affinity. It is also employed in material science for creating advanced polymers and functional materials with tailored properties.
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