[3-(Methoxycarbamoyl)phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that also contains a methoxycarbamoyl substituent. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The methoxycarbamoyl group enhances its solubility and reactivity, allowing for potential use in drug development and as a building block in the synthesis of more complex molecules. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds. The compound's structure suggests it may participate in hydrogen bonding due to the presence of the boronic acid and the amide functionalities, influencing its physical properties such as melting point and solubility in different solvents. Overall, [3-(methoxycarbamoyl)phenyl]boronic acid is a versatile compound with significant implications in chemical research and development.

[3-(methoxycarbamoyl)phenyl]boronic acid

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(3-(Methoxycarbamoyl)phenyl)boronic acid

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CAS 850567-26-9: [3-(methoxycarbamoyl)phenyl]boronic acid

(3-(Methoxycarbamoyl)phenyl)boronic acid

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