Boronic acid, specifically B-[4-chloro-3-[(ethylamino)carbonyl]phenyl]- (CAS 871332-69-3), is an organic compound characterized by the presence of a boron atom bonded to a phenyl group that features a chloro substituent and an ethylamino carbonyl group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible complexes with diols, which is useful in various applications including organic synthesis and medicinal chemistry. The presence of the chloro group can influence its reactivity and solubility, while the ethylamino carbonyl moiety may enhance its biological activity or interaction with specific targets. Boronic acids are known for their role in Suzuki coupling reactions, making them valuable in the synthesis of complex organic molecules. Additionally, the compound may exhibit specific physical properties such as melting point and solubility that are influenced by its molecular structure. Overall, this compound is of interest in both academic research and potential pharmaceutical applications due to its unique functional groups and reactivity.

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

871332-69-3: Boronic acid, specifically B-[4-chloro-3-[(ethylamino)carbonyl]phenyl]- (CAS 871332-69-3), is an organic compound characterized by the presence of a boron atom bonded to a phenyl group that features a chloro substituent and an ethylamino carbonyl group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible complexes with diols, which is useful in various applications including organic synthesis and medicinal chemistry. The presence of the chloro group can influence its reactivity and solubility, while the ethylamino carbonyl moiety may enhance its biological activity or interaction with specific targets. Boronic acids are known for their role in Suzuki coupling reactions, making them valuable in the synthesis of complex organic molecules. Additionally, the compound may exhibit specific physical properties such as melting point and solubility that are influenced by its molecular structure. Overall, this compound is of interest in both academic research and potential pharmaceutical applications due to its unique functional groups and reactivity.

4-Chloro-3-(ethylcarbamoyl)phenylboronic acid

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

CAS 871332-69-3

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

4-Chloro-3-(ethylcarbamoyl)phenylboronic acid

Ref: IN-DA004OT3

4-Chloro-3-(ethylcarbamoyl)phenylboronic acid

Ref: 54-OR360078

(4-Chloro-3-(ethylcarbamoyl)phenyl)boronic acid

Ref: 10-F215793