[4-Fluoro-3-(propylcarbamoyl)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 organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a fluorine atom and a propylcarbamoyl group, which contributes to its unique chemical properties and potential biological activity. The presence of the boronic acid moiety allows for participation in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds. Additionally, the fluorine substitution can enhance the compound's lipophilicity and influence its interaction with biological targets. This compound may exhibit specific solubility characteristics in polar and non-polar solvents, and its reactivity can be influenced by the electronic effects of the substituents on the aromatic ring. Overall, [4-fluoro-3-(propylcarbamoyl)phenyl]boronic acid represents a versatile building block in synthetic chemistry and drug development.

[4-fluoro-3-(propylcarbamoyl)phenyl]boronic acid

874219-32-6: [4-Fluoro-3-(propylcarbamoyl)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 organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a fluorine atom and a propylcarbamoyl group, which contributes to its unique chemical properties and potential biological activity. The presence of the boronic acid moiety allows for participation in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds. Additionally, the fluorine substitution can enhance the compound's lipophilicity and influence its interaction with biological targets. This compound may exhibit specific solubility characteristics in polar and non-polar solvents, and its reactivity can be influenced by the electronic effects of the substituents on the aromatic ring. Overall, [4-fluoro-3-(propylcarbamoyl)phenyl]boronic acid represents a versatile building block in synthetic chemistry and drug development.

CAS 874219-32-6

[4-fluoro-3-(propylcarbamoyl)phenyl]boronic acid

4-FLUORO-3-(N-PROPYLCARBAMOYL)BENZENEBORONIC ACID

Ref: IN-DA004J9P

4-Fluoro-3-(propylcarbamoyl)benzeneboronic acid

Ref: 54-PC4988

(4-Fluoro-3-(propylcarbamoyl)phenyl)boronic acid

Ref: 10-F219688