2,6-Dimethyl-4-methoxyphenylboronic 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 methyl and methoxy groups. This compound typically exhibits a white to off-white crystalline solid form and is soluble in polar organic solvents, such as methanol and ethanol, due to the presence of the boronic acid moiety. The presence of the methoxy group enhances its electron-donating properties, which can influence its reactivity in various chemical reactions, particularly in Suzuki coupling reactions, where it acts as a nucleophile. The methyl groups provide steric hindrance, which can affect the compound's reactivity and selectivity in synthetic applications. Additionally, boronic acids are known for their ability to form reversible complexes with diols, making them useful in various applications, including drug development and materials science. Overall, 2,6-Dimethyl-4-methoxyphenylboronic acid is a versatile compound with significant utility in organic synthesis and medicinal chemistry.

2,6-Dimethyl-4-methoxyphenylboronic acid

361543-99-9: 4-Methoxy-2,6-dimethylphenylboronic acid, (2,6-Dimethyl-4-Methoxyphenyl)Boronic Acid

2,6-Dimethyl-4-methoxybenzeneboronic acid

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CAS 361543-99-9: 2,6-Dimethyl-4-methoxyphenylboronic acid

2,6-Dimethyl-4-methoxybenzeneboronic acid

Ref: 54-OR7207

(2,6-Dimethyl-4-methoxyphenyl)boronic acid

Ref: 3D-FD31426

4-Methoxy-2,6-dimethylphenylboronic Acid (contains varying amounts of Anhydride)

Ref: 3B-M2244

4-Methoxy-2,6-dimethylphenylboronic acid

Ref: IN-DA0032BZ

2,6-Dimethyl-4-methoxybenzeneboronic acid

Ref: 10-F065580