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CAS 864772-18-9

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Phenoxyphenyl-3-boronic acid pinacol ester

Description:
Phenoxyphenyl-3-boronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group esterified with pinacol, along with phenoxy and phenyl substituents. This compound typically exhibits a white to off-white solid appearance and is soluble in organic solvents such as dichloromethane and ethanol, but may have limited solubility in water. The boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and materials science. Its structure contributes to its reactivity, enabling it to form complexes with diols and other Lewis bases. Additionally, the presence of the phenoxy and phenyl groups can influence its electronic properties and steric hindrance, affecting its reactivity and interactions with other molecules. As with many boronic acid derivatives, it is important to handle this compound with care, as boron-containing compounds can exhibit specific toxicity and environmental considerations.
Formula:C18H21BO3
Synonyms:
  • 4,4,5,5-Tetramethyl-2-(3-phenoxyphenyl)-1,3,2-dioxaborolane
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