3-Acetamido-5-carboxybenzeneboronic acid, with the CAS number 108749-15-1, is a boronic acid derivative characterized by the presence of both an acetamido group and a carboxylic acid group attached to a benzene ring. 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 presence of the acetamido group enhances its solubility in polar solvents, while the carboxylic acid group contributes to its acidity and potential reactivity. The compound is often utilized in the development of pharmaceuticals and as a building block in the synthesis of more complex organic molecules. Its boronic acid functionality allows for participation in Suzuki-Miyaura cross-coupling reactions, which are pivotal in forming carbon-carbon bonds. Overall, 3-acetamido-5-carboxybenzeneboronic acid is a versatile compound with significant implications in both research and industrial applications.

3-ACETAMIDO-5-CARBOXYBENZENEBORONIC ACID 98

108749-15-1: (3-Acetamido-5-carboxy)phenylboronic acid, 3-Acetamido-5-Borono-Benzoic Acid, 3-Acetamido-5-Carboxybenzeneboronic Acid, 3-Acetamido-5-carboxybenzeneboronic acid 98%

3-Acetamido-5-carboxybenzeneboronic acid

3-Acetamido-5-boronobenzoic acid

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CAS 108749-15-1: 3-ACETAMIDO-5-CARBOXYBENZENEBORONIC ACID 98

3-Acetamido-5-carboxybenzeneboronic acid

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3-Acetamido-5-boronobenzoic acid

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3-Acetamido-5-boronobenzoic acid

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3-Acetamido-5-boronobenzoic acid

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