Boronic acids are a class of organic compounds characterized by the presence of a boron atom bonded to a hydroxyl group and an organic substituent. The specific compound "Boronic acid, B-(2-fluoro-6-propoxy-3-pyridinyl)-" features a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom. The presence of a fluorine atom at the 2-position and a propoxy group at the 6-position of the pyridine ring contributes to its unique chemical properties, potentially influencing its reactivity and solubility. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them useful in various applications, including organic synthesis and medicinal chemistry. They can participate in Suzuki coupling reactions, which are valuable for constructing carbon-carbon bonds. The specific structure of this boronic acid may also impart distinct biological activity, making it of interest in pharmaceutical research. Overall, the characteristics of this compound are defined by its boron functionality, aromatic nature, and the influence of its substituents on chemical behavior.

Boronic acid, B-(2-fluoro-6-propoxy-3-pyridinyl)-

2096338-78-0: Boronic acids are a class of organic compounds characterized by the presence of a boron atom bonded to a hydroxyl group and an organic substituent. The specific compound "Boronic acid, B-(2-fluoro-6-propoxy-3-pyridinyl)-" features a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom. The presence of a fluorine atom at the 2-position and a propoxy group at the 6-position of the pyridine ring contributes to its unique chemical properties, potentially influencing its reactivity and solubility. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them useful in various applications, including organic synthesis and medicinal chemistry. They can participate in Suzuki coupling reactions, which are valuable for constructing carbon-carbon bonds. The specific structure of this boronic acid may also impart distinct biological activity, making it of interest in pharmaceutical research. Overall, the characteristics of this compound are defined by its boron functionality, aromatic nature, and the influence of its substituents on chemical behavior.

CAS 2096338-78-0

Boronic acid, B-(2-fluoro-6-propoxy-3-pyridinyl)-

2-Fluoro-6-propoxypyridine-3-boronic acid

Ref: IN-DA01EHKO

2-Fluoro-6-propoxypyridine-3-boronic acid

Ref: 54-PC901347

2-Fluoro-6-propoxypyridine-3-boronic acid

Ref: 10-F623509