[3-Methoxy-4-(methoxycarbonyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a phenyl ring substituted with both a methoxy group and a methoxycarbonyl group, enhancing its solubility and reactivity. The methoxy group contributes to the electron-donating properties, while the methoxycarbonyl group introduces a carbonyl functionality that can participate in various chemical reactions, such as esterification or acylation. The boronic acid moiety allows for applications in Suzuki coupling reactions, making it valuable in organic synthesis and materials science. Additionally, this compound may exhibit interesting biological activities, as boronic acids are often explored for their potential in medicinal chemistry. Its stability, solubility in organic solvents, and reactivity with nucleophiles make it a versatile building block in the synthesis of complex organic molecules.

[3-methoxy-4-(methoxycarbonyl)phenyl]boronic acid

603122-41-4: Benzoic Acid, 4-Borono-2-Methoxy-, Methyl Ester, 3-Methoxy-4-methoxycarbonylphenylboronic acid

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CAS 603122-41-4: [3-methoxy-4-(methoxycarbonyl)phenyl]boronic acid

3-Methoxy-4-methoxycarbonylphenylboronicacid

Ref: 3D-FM149408

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3-METHOXY-4-METHOXYCARBONYLPHENYLBORONIC ACID

Ref: IN-DA00EA07

3-Methoxy-4-methoxycarbonylphenylboronic acid

Ref: 10-F219495