Description:4-T-Butoxyphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a tert-butoxy group. This compound typically appears as a white to off-white solid and is soluble in organic solvents such as dichloromethane and ethanol, but has limited solubility in water due to its hydrophobic tert-butoxy substituent. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and as a reagent in Suzuki coupling reactions. Additionally, the presence of the tert-butoxy group can influence the compound's reactivity and stability, enhancing its utility in medicinal chemistry and materials science. Safety data should be consulted for handling, as boronic acids can be sensitive to moisture and may require specific storage conditions. Overall, 4-T-butoxyphenylboronic acid is a versatile compound with significant relevance in synthetic organic chemistry.
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