5-Borono-2-pyridinecarboxylic acid is an organic compound characterized by its boronic acid functional group and a pyridine ring. It features a boron atom bonded to a hydroxyl group and a carbon atom, which is part of a carboxylic acid group, making it a versatile building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The presence of the pyridine ring contributes to its aromatic properties and potential for coordination with metal ions, enhancing its utility in catalysis and material science. This compound is typically a white to off-white solid and is soluble in polar solvents, such as water and alcohols, due to the presence of the carboxylic acid group. Its reactivity is influenced by the boron atom, which can participate in various coupling reactions, such as Suzuki-Miyaura cross-coupling, making it valuable in the synthesis of complex organic molecules. Overall, 5-Borono-2-pyridinecarboxylic acid is an important compound in modern organic chemistry with diverse applications.

5-Borono-2-pyridinecarboxylic acid

913836-11-0: 2-Carboxypyridine-5-boronic acid, 2-Pyridinecarboxylic acid, 5-borono-, 5-Borono-2-pyridinecarboxylic acid, 5-Boronopicolinic Acid

CAS 913836-11-0: 5-Borono-2-pyridinecarboxylic acid

5-Boronopicolinic acid

Ref: IN-DA006N8O

6-Carboxypyridine-3-boronic acid

Ref: 54-OR3781

5-Boronopicolinic acid

Ref: 10-F231168

5-Boronopicolinic Acid

Ref: TR-B689488