4-Bromo-2-methoxyphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that also contains a bromine atom and a methoxy group. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the boronic acid functionality. It is known for its utility in organic synthesis, particularly in Suzuki coupling reactions, where it serves as a versatile building block for the formation of carbon-carbon bonds. The presence of the bromine atom enhances its reactivity, while the methoxy group can influence the electronic properties of the molecule, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in various applications, including sensing and drug delivery systems. Overall, 4-Bromo-2-methoxyphenylboronic acid is a significant compound in the field of organic chemistry.

4-Bromo-2-methoxyphenylboronic acid

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CAS 889849-21-2: 4-Bromo-2-methoxyphenylboronic acid

4-Bromo-2-methoxyphenylboronic acid

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4-Bromo-2-methoxyphenylboronic acid

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4-Bromo-2-methoxyphenylboronic acid

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(4-Bromo-2-methoxyphenyl)boronic acid

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