[3-Fluoro-4-(pyrrolidine-1-carbonyl)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 applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a fluorine atom and a pyrrolidine-1-carbonyl group, contributing to its unique chemical properties and potential biological activity. The presence of the boronic acid moiety allows for participation in Suzuki coupling reactions, which are valuable in the formation of carbon-carbon bonds. Additionally, the fluorine atom can influence the compound's electronic properties and lipophilicity, potentially affecting its pharmacokinetics and interactions with biological targets. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their relevance in drug discovery and development.

[3-fluoro-4-(pyrrolidine-1-carbonyl)phenyl]boronic acid

874289-09-5: [3-Fluoro-4-(pyrrolidin-1-ylcarbonyl)phenyl]boronic acid, boronic acid, B-[3-fluoro-4-(1-pyrrolidinylcarbonyl)phenyl]-

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[3-fluoro-4-(pyrrolidine-1-carbonyl)phenyl]boronic Acid

(3-Fluoro-4-(pyrrolidine-1-carbonyl)phenyl)boronic acid

3-Fluoro-4-(pyrrolidin-1-ylcarbonyl)benzeneboronic acid

CAS 874289-09-5: [3-fluoro-4-(pyrrolidine-1-carbonyl)phenyl]boronic acid

[3-fluoro-4-(pyrrolidine-1-carbonyl)phenyl]boronic Acid

Ref: 3D-FF105791

(3-Fluoro-4-(pyrrolidine-1-carbonyl)phenyl)boronic acid

Ref: IN-DA004G4M

(3-Fluoro-4-(pyrrolidine-1-carbonyl)phenyl)boronic acid

Ref: 10-F691526

3-Fluoro-4-(pyrrolidin-1-ylcarbonyl)benzeneboronic acid

Ref: 54-PC3535