2-Fluoro-6-phenyl-3-pyridineboronic 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 and other nucleophiles. This compound features a pyridine ring substituted with a fluorine atom and a phenyl group, contributing to its unique electronic and steric properties. The presence of the boronic acid moiety allows it to participate in various chemical reactions, including Suzuki-Miyaura cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry. Its solubility in polar solvents and stability under standard laboratory conditions are typical for boronic acids. Additionally, the fluorine substitution can enhance the compound's reactivity and influence its biological activity, making it a subject of interest in drug development and materials science. Overall, 2-fluoro-6-phenyl-3-pyridineboronic acid exemplifies the versatility of boron-containing compounds in synthetic chemistry.

2-FLUORO-6-PHENYL-3-PYRIDINEBORONIC ACID

1029654-19-0: 2-Fluoro-6-phenyl-3-pyridineboronic 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 and other nucleophiles. This compound features a pyridine ring substituted with a fluorine atom and a phenyl group, contributing to its unique electronic and steric properties. The presence of the boronic acid moiety allows it to participate in various chemical reactions, including Suzuki-Miyaura cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry. Its solubility in polar solvents and stability under standard laboratory conditions are typical for boronic acids. Additionally, the fluorine substitution can enhance the compound's reactivity and influence its biological activity, making it a subject of interest in drug development and materials science. Overall, 2-fluoro-6-phenyl-3-pyridineboronic acid exemplifies the versatility of boron-containing compounds in synthetic chemistry.

CAS 1029654-19-0

2-FLUORO-6-PHENYL-3-PYRIDINEBORONIC ACID

2-Fluoro-6-phenylpyridine-3-boronic Acid

Ref: IN-DA003BN9

2-Fluoro-6-phenylpyridine-3-boronic acid

Ref: 54-PC412209