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CAS 957120-49-9

:

B-[3-Chloro-5-[(ethylamino)carbonyl]phenyl]boronic acid

Description:
B-[3-Chloro-5-[(ethylamino)carbonyl]phenyl]boronic acid, with the CAS number 957120-49-9, is a boronic acid derivative characterized by its boron atom bonded to a phenyl group that is substituted with a chlorine atom and an ethylamino 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 and ethylamino carbonyl substituents can influence its reactivity and solubility, potentially enhancing its biological activity or selectivity in chemical reactions. Boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, this compound may exhibit specific interactions with biological targets, making it of interest in drug development and research related to cancer therapies or other diseases. Its stability, solubility, and reactivity can vary based on the conditions and solvents used in experiments.
Formula:C9H11BClNO3
InChI:InChI=1S/C9H11BClNO3/c1-2-12-9(13)6-3-7(10(14)15)5-8(11)4-6/h3-5,14-15H,2H2,1H3,(H,12,13)
InChI key:InChIKey=RDZMWYYVLMBINL-UHFFFAOYSA-N
SMILES:C(NCC)(=O)C1=CC(B(O)O)=CC(Cl)=C1
Synonyms:
  • 3-Chloro-5-(ethylcarbamoyl)phenylboronic acid
  • B-[3-Chloro-5-[(ethylamino)carbonyl]phenyl]boronic acid
  • N-Ethyl 3-borono-5-chlorobenzamide
  • Boronic acid, B-[3-chloro-5-[(ethylamino)carbonyl]phenyl]-
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