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CAS 1860005-05-5

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3-Chloro-4-(cyclopropylmethoxy)phenylboronic acid, pinacol ester

Description:
3-Chloro-4-(cyclopropylmethoxy)phenylboronic acid, pinacol ester, is an organoboron compound characterized by the presence of a boronic acid functional group and a pinacol ester moiety. This compound features a chlorinated phenyl ring, which enhances its reactivity and solubility in organic solvents. The cyclopropylmethoxy group contributes to its steric and electronic properties, potentially influencing its reactivity in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is commonly utilized in organic synthesis for forming carbon-carbon bonds. The pinacol ester formation provides stability and solubility, making it easier to handle and store. This compound is typically used in medicinal chemistry and materials science, where boron-containing compounds play a crucial role in drug development and the synthesis of complex organic molecules. Its unique structure allows for various applications, including in the development of pharmaceuticals and agrochemicals. As with many boronic acids and their derivatives, it is important to consider its reactivity with diols and its potential applications in sensor technology and catalysis.
Formula:C16H22BClO3
Synonyms:
  • 1,3,2-Dioxaborolane, 2-[3-chloro-4-(cyclopropylmethoxy)phenyl]-4,4,5,5-tetramethyl-
  • 3-Chloro-4-(cyclopropylmethoxy)phenylboronic acid, pinacol ester
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