(2-(2-(trifluoromethyl)phenyl)pyrimidin-5-yl)boronic acid
95%
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This compound is widely utilized in the field of organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the creation of complex molecules, especially in the pharmaceutical industry, where it is used to develop active pharmaceutical ingredients (APIs). Its boronic acid group enables efficient coupling with aryl halides or triflates, facilitating the synthesis of biaryl structures, which are common in many drugs. The pyrimidine core substituted with a 2-(trifluoromethyl)phenyl group at the 2-position imparts unique chemical and biological properties, such as enhanced selectivity and potential for improved pharmacokinetics, making it valuable for synthesizing compounds with interesting chemical and biological attributes. Additionally, it finds applications in material science for the development of organic electronic materials, where its unique structure contributes to the design of advanced polymers and small molecules for optoelectronic devices.
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