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CAS 1027757-13-6

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2-BENZYLOXYPHENYLBORONIC ACID, PINACOL ESTER

Description:
2-Benzyloxyphenylboronic acid, pinacol ester, is an organoboron compound characterized by the presence of a boronic acid functional group and a pinacol ester moiety. This compound typically exhibits a white to off-white solid appearance and is soluble in organic solvents such as dichloromethane and ethyl acetate, while being less soluble in water. The boronic acid group allows for reversible covalent bonding with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. Its structure features a phenyl ring substituted with a benzyloxy group, which can enhance its reactivity and stability. The pinacol ester formation provides additional protection to the boronic acid, facilitating its use in cross-coupling reactions, such as Suzuki-Miyaura coupling. This compound is of interest in the development of pharmaceuticals and materials science due to its ability to form complexes with various substrates. Safety data should be consulted for handling, as organoboron compounds can exhibit varying degrees of toxicity and reactivity.
Formula:C19H23BO3
Synonyms:
  • 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[2-(phenylmethoxy)phenyl]-
  • 2-BENZYLOXYPHENYLBORONIC ACID, PINACOL ESTER ISO 9001：2015 REACH
  • 2-(2-Benzyloxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 2-Benzyloxyphenylboronic acid pinacol ester
  • 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyloxybenzene
  • 2-(2-BENZYLOXYPHENYL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE
  • 2-BENZYLOXYPHENYLBORONIC ACID, PINACOL ESTER
  • AKOS BRN-1151
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