CAS 475250-54-5
:2-(Trifluoromethyl)benzylboronic acid pinacol ester
Description:
2-(Trifluoromethyl)benzylboronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group and a trifluoromethyl-substituted benzyl moiety. This compound typically exhibits a white to off-white solid appearance and is soluble in organic solvents such as dichloromethane and tetrahydrofuran. The trifluoromethyl group enhances its electronic properties, making it useful in various chemical reactions, particularly in cross-coupling reactions like Suzuki-Miyaura coupling, where it serves as a key intermediate for synthesizing complex organic molecules. The pinacol ester moiety provides stability and solubility, facilitating its use in synthetic applications. Additionally, the compound may exhibit unique reactivity patterns due to the presence of both the boron atom and the electron-withdrawing trifluoromethyl group, which can influence its behavior in chemical transformations. Safety data should be consulted, as organoboron compounds can have specific handling and toxicity considerations. Overall, this compound is valuable in organic synthesis and materials science, particularly in the development of pharmaceuticals and agrochemicals.
Formula:C14H18BF3O2
Synonyms:- 2-(2-(Trifluoromethyl)benzyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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