(2-Fluoro-4-(MorpholinoMethyl)phenyl)boronic 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, making it useful in various applications, including medicinal chemistry and organic synthesis. The compound features a fluorine atom at the ortho position relative to the boronic acid group, which can influence its electronic properties and reactivity. The morpholino group, a cyclic amine, enhances the compound's solubility and may contribute to its biological activity. This compound is typically a white to off-white solid and is soluble in polar solvents. Its boronic acid functionality allows it to participate in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the presence of the morpholino group may impart specific pharmacological properties, making it of interest in drug development. Overall, this compound exemplifies the versatility of boronic acids in both synthetic and medicinal chemistry contexts.

(2-fluoro-4-(MorpholinoMethyl)phenyl)boronic acid

1451393-46-6: (2-Fluoro-4-(MorpholinoMethyl)phenyl)boronic 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, making it useful in various applications, including medicinal chemistry and organic synthesis. The compound features a fluorine atom at the ortho position relative to the boronic acid group, which can influence its electronic properties and reactivity. The morpholino group, a cyclic amine, enhances the compound's solubility and may contribute to its biological activity. This compound is typically a white to off-white solid and is soluble in polar solvents. Its boronic acid functionality allows it to participate in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the presence of the morpholino group may impart specific pharmacological properties, making it of interest in drug development. Overall, this compound exemplifies the versatility of boronic acids in both synthetic and medicinal chemistry contexts.

CAS 1451393-46-6

(2-fluoro-4-(MorpholinoMethyl)phenyl)boronic acid

Boronic acid, B-[2-fluoro-4-(4-morpholinylmethyl)phenyl]-

Ref: IN-DA01FFYJ

2-Fluoro-4-(morpholinomethyl)phenylboronic acid

Ref: 10-F627911