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CAS 1352426-91-5

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5-Chloro-2-Methylphenylboronic acid, pinacol ester

Description:
5-Chloro-2-Methylphenylboronic acid, pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group that is esterified with pinacol. This compound typically features a chlorinated aromatic ring, which contributes to its reactivity and potential applications in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. The pinacol ester moiety enhances the stability of the boron center, making it more suitable for various chemical transformations. In terms of solubility, compounds of this nature are often soluble in organic solvents, which facilitates their use in laboratory settings. The presence of the chlorine atom can influence the electronic properties of the molecule, potentially affecting its reactivity and interactions with other chemical species. Overall, 5-Chloro-2-Methylphenylboronic acid, pinacol ester is a valuable intermediate in the synthesis of complex organic molecules, particularly in the fields of medicinal chemistry and materials science.
Formula:C13H18BClO2
Synonyms:
  • 2-(5-chloro-2-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 5-Chloro-2-Methylphenylboronic acid, pinacol ester
  • 1,3,2-Dioxaborolane, 2-(5-chloro-2-methylphenyl)-4,4,5,5-tetramethyl-
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