3,5-Pyridine diboronic acid, with the CAS number 1012085-48-1, is an organoboron compound characterized by the presence of two boronic acid groups attached to a pyridine ring. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, owing to the presence of the boronic acid functional groups. The diboronic acid structure allows for the formation of stable complexes with various substrates, making it useful in organic synthesis and materials science, particularly in the development of boron-containing polymers and ligands for catalysis. Additionally, 3,5-pyridine diboronic acid can participate in cross-coupling reactions, which are essential in the formation of carbon-carbon bonds in organic chemistry. Its reactivity is influenced by the acidity of the boronic acid groups, which can undergo transformations under specific conditions, such as oxidation or coupling with other organic molecules. Overall, this compound serves as a valuable building block in synthetic chemistry and has potential applications in medicinal chemistry and materials development.

3,5-Pridine diboronic acid

1012085-48-1: 3,5-Pyridine diboronic acid, with the CAS number 1012085-48-1, is an organoboron compound characterized by the presence of two boronic acid groups attached to a pyridine ring. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, owing to the presence of the boronic acid functional groups. The diboronic acid structure allows for the formation of stable complexes with various substrates, making it useful in organic synthesis and materials science, particularly in the development of boron-containing polymers and ligands for catalysis. Additionally, 3,5-pyridine diboronic acid can participate in cross-coupling reactions, which are essential in the formation of carbon-carbon bonds in organic chemistry. Its reactivity is influenced by the acidity of the boronic acid groups, which can undergo transformations under specific conditions, such as oxidation or coupling with other organic molecules. Overall, this compound serves as a valuable building block in synthetic chemistry and has potential applications in medicinal chemistry and materials development.

CAS 1012085-48-1

3,5-Pridine diboronic acid

Pyridine-3,5-diyldiboronic acid

Ref: IN-DA0003YR

Pyridine-3,5-diyldiboronic acid

Ref: 10-F735663