[2-Fluoro-5-(hydrazinecarbonyl)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 and play a significant role in Suzuki coupling reactions. The compound features a phenyl ring substituted with a fluorine atom and a hydrazinecarbonyl group, which contributes to its reactivity and potential biological activity. The presence of the hydrazine moiety may impart unique properties, such as the ability to participate in hydrazone formation or act as a potential ligand in coordination chemistry. Additionally, boronic acids are often utilized in medicinal chemistry for drug development due to their ability to interact with biological targets. The compound's solubility, stability, and reactivity can be influenced by the electronic effects of the fluorine atom and the hydrazinecarbonyl group, making it a subject of interest in both synthetic and medicinal chemistry. Overall, [2-fluoro-5-(hydrazinecarbonyl)phenyl]boronic acid exemplifies the diverse applications of boronic acids in chemical research.

[2-fluoro-5-(hydrazinecarbonyl)phenyl]boronic acid

874289-56-2: [2-Fluoro-5-(hydrazinecarbonyl)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 and play a significant role in Suzuki coupling reactions. The compound features a phenyl ring substituted with a fluorine atom and a hydrazinecarbonyl group, which contributes to its reactivity and potential biological activity. The presence of the hydrazine moiety may impart unique properties, such as the ability to participate in hydrazone formation or act as a potential ligand in coordination chemistry. Additionally, boronic acids are often utilized in medicinal chemistry for drug development due to their ability to interact with biological targets. The compound's solubility, stability, and reactivity can be influenced by the electronic effects of the fluorine atom and the hydrazinecarbonyl group, making it a subject of interest in both synthetic and medicinal chemistry. Overall, [2-fluoro-5-(hydrazinecarbonyl)phenyl]boronic acid exemplifies the diverse applications of boronic acids in chemical research.

CAS 874289-56-2

[2-fluoro-5-(hydrazinecarbonyl)phenyl]boronic acid

3-Borono-4-fluorobenzohydrazide

Ref: IN-DA004J06

2-Fluoro-5-(hydrazinocarbonyl)benzeneboronic acid

Ref: 54-PC3561

(2-Fluoro-5-(hydrazinecarbonyl)phenyl)boronic acid

Ref: 10-F692471