[3-(Diethylcarbamoyl)-4-fluoro-phenyl]boronic acid is an organic 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 chemical reactions, including Suzuki coupling. The compound features a phenyl ring substituted with a fluorine atom and a diethylcarbamoyl group, which enhances its solubility and reactivity. The diethylcarbamoyl moiety contributes to the compound's overall polarity and can influence its interaction with biological systems, potentially making it relevant in medicinal chemistry. The boronic acid functionality allows for participation in cross-coupling reactions, which are pivotal in the synthesis of complex organic molecules. Additionally, the presence of the fluorine atom may impart unique electronic properties, affecting the compound's reactivity and stability. Overall, this compound exemplifies the versatility of boronic acids in organic synthesis and their potential applications in drug development and material science.

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

874219-28-0: [3-(Diethylcarbamoyl)-4-fluoro-phenyl]boronic acid is an organic 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 chemical reactions, including Suzuki coupling. The compound features a phenyl ring substituted with a fluorine atom and a diethylcarbamoyl group, which enhances its solubility and reactivity. The diethylcarbamoyl moiety contributes to the compound's overall polarity and can influence its interaction with biological systems, potentially making it relevant in medicinal chemistry. The boronic acid functionality allows for participation in cross-coupling reactions, which are pivotal in the synthesis of complex organic molecules. Additionally, the presence of the fluorine atom may impart unique electronic properties, affecting the compound's reactivity and stability. Overall, this compound exemplifies the versatility of boronic acids in organic synthesis and their potential applications in drug development and material science.

CAS 874219-28-0

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

(3-Diethylaminocarbonyl-4-fluorobenzene)boronic acid

Ref: IN-DA0036BR

3-(Diethylcarbamoyl)-4-fluorobenzeneboronic acid

Ref: 54-PC4997

(3-(Diethylcarbamoyl)-4-fluorophenyl)boronic acid

Ref: 10-F219685