Boronic acid, specifically B-[4-chloro-3-(4-morpholinylcarbonyl)phenyl]- (CAS 871332-71-7), is an organoboron compound characterized by the presence of a boron atom bonded to a phenyl group that features a chloro substituent and a morpholinylcarbonyl 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 enhance its reactivity and solubility in organic solvents, while the morpholine ring may contribute to its biological activity and interaction with biological targets. Boronic acids are often utilized in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the structural features of this compound suggest potential applications in drug development, particularly in the design of inhibitors or modulators of biological pathways. Overall, this compound exemplifies the versatility and utility of boronic acids in chemical research and industry.

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

871332-71-7: Boronic acid, specifically B-[4-chloro-3-(4-morpholinylcarbonyl)phenyl]- (CAS 871332-71-7), is an organoboron compound characterized by the presence of a boron atom bonded to a phenyl group that features a chloro substituent and a morpholinylcarbonyl 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 enhance its reactivity and solubility in organic solvents, while the morpholine ring may contribute to its biological activity and interaction with biological targets. Boronic acids are often utilized in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the structural features of this compound suggest potential applications in drug development, particularly in the design of inhibitors or modulators of biological pathways. Overall, this compound exemplifies the versatility and utility of boronic acids in chemical research and industry.

(4-Chloro-3-(morpholine-4-carbonyl)phenyl)boronic acid

<p>4-Chloro-3-(N-morpholinecarbonyl)phenylboronic acid</p>

CAS 871332-71-7

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

(4-Chloro-3-(morpholine-4-carbonyl)phenyl)boronic acid

Ref: IN-DA0036ET

4-Chloro-3-(N-morpholinecarbonyl)phenylboronic acid

Ref: 54-OR360063

(4-Chloro-3-(morpholine-4-carbonyl)phenyl)boronic acid

Ref: 10-F216089