Boronic acid, specifically B-[3-chloro-5-[(dimethylamino)carbonyl]phenyl]- (CAS 957120-57-9), is an organoboron compound characterized by the presence of a boron atom bonded to a phenyl group that contains a chloro substituent and a dimethylamino carbonyl group. 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 dimethylamino carbonyl moiety may enhance its biological activity or facilitate interactions with biological targets. Boronic acids are often utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the compound's structure suggests potential applications in drug development, particularly in the design of inhibitors or modulators of biological pathways. Overall, this compound exemplifies the diverse functionality and utility of boronic acids in chemical research and industry.

Boronic acid,B-[3-chloro-5-[(dimethylamino)carbonyl]phenyl]-

957120-57-9: [3-Chloro-5-(dimethylcarbamoyl)phenyl]boronicacid

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N-Dimethyl 3-borono-5-chlorobenzamide

(3-Chloro-5-(dimethylcarbamoyl)phenyl)boronic acid

3-Chloro-5-(dimethylcarbamoyl)benzeneboronic acid

CAS 957120-57-9: Boronic acid,B-[3-chloro-5-[(dimethylamino)carbonyl]phenyl]-

N-Dimethyl 3-borono-5-chlorobenzamide

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Boronic acid,B-[3-chloro-5-[(dimethylamino)carbonyl]phenyl]-

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(3-Chloro-5-(dimethylcarbamoyl)phenyl)boronic acid

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3-Chloro-5-(dimethylcarbamoyl)benzeneboronic acid

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