Boronic acid, specifically B-[4-chloro-3-(1-pyrrolidinylcarbonyl)phenyl]- (CAS 871332-75-1), is an organic compound characterized by the presence of a boron atom bonded to a phenyl group that features a chloro substituent and a pyrrolidinylcarbonyl moiety. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the chloro group can influence its reactivity and solubility, while the pyrrolidinylcarbonyl group may enhance its biological activity or facilitate interactions with biological targets. Boronic acids are often utilized in the development of pharmaceuticals and as intermediates in the synthesis of complex organic molecules. Additionally, they can participate in Suzuki coupling reactions, which are valuable in constructing carbon-carbon bonds in organic synthesis. Overall, this compound's unique structure and functional groups contribute to its potential utility in chemical research and applications.

Boronic acid,B-[4-chloro-3-(1-pyrrolidinylcarbonyl)phenyl]-

871332-75-1: Boronic acid, specifically B-[4-chloro-3-(1-pyrrolidinylcarbonyl)phenyl]- (CAS 871332-75-1), is an organic compound characterized by the presence of a boron atom bonded to a phenyl group that features a chloro substituent and a pyrrolidinylcarbonyl moiety. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the chloro group can influence its reactivity and solubility, while the pyrrolidinylcarbonyl group may enhance its biological activity or facilitate interactions with biological targets. Boronic acids are often utilized in the development of pharmaceuticals and as intermediates in the synthesis of complex organic molecules. Additionally, they can participate in Suzuki coupling reactions, which are valuable in constructing carbon-carbon bonds in organic synthesis. Overall, this compound's unique structure and functional groups contribute to its potential utility in chemical research and applications.

CAS 871332-75-1

Boronic acid,B-[4-chloro-3-(1-pyrrolidinylcarbonyl)phenyl]-

4-Chloro-3-(pyrrolidine-1-carbonyl)phenylboronic acid

Ref: IN-DA004OT1

4-Chloro-3-(pyrrolidine-1-carbonyl)phenylboronic acid

Ref: 54-OR360060

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

Ref: 10-F216105