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CAS 871332-76-2

:

B-[4-Chloro-3-[(dimethylamino)carbonyl]phenyl]boronic acid

Description:
B-[4-Chloro-3-[(dimethylamino)carbonyl]phenyl]boronic acid, with the CAS number 871332-76-2, is a boronic acid derivative characterized by its boron atom bonded to a phenyl ring that contains a chloro substituent and a dimethylaminocarbonyl 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 enhances its reactivity and potential for further functionalization. Additionally, the dimethylaminocarbonyl moiety contributes to its solubility and stability in organic solvents. This compound may also exhibit biological activity, making it of interest in drug discovery and development. Its structural features suggest potential applications in the development of inhibitors or modulators in biochemical pathways, particularly in the context of cancer research and other therapeutic areas. As with many boronic acids, careful handling and storage are recommended due to their sensitivity to moisture and air.
Formula:C9H11BClNO3
InChI:InChI=1S/C9H11BClNO3/c1-12(2)9(13)7-5-6(10(14)15)3-4-8(7)11/h3-5,14-15H,1-2H3
InChI key:InChIKey=ZTPXXLBYJKNIDH-UHFFFAOYSA-N
SMILES:C(N(C)C)(=O)C1=CC(B(O)O)=CC=C1Cl
Synonyms:
  • (4-Chloro-3-(dimethylaminocarbonyl)phenyl)boronic acid
  • (4-Chloro-3-(dimethylcarbamoyl)phenyl)boronicacid
  • B-[4-Chloro-3-[(dimethylamino)carbonyl]phenyl]boronic acid
  • Boronic acid, B-[4-chloro-3-[(dimethylamino)carbonyl]phenyl]-
  • Boronic acid, [4-chloro-3-[(dimethylamino)carbonyl]phenyl]-
  • [4-Chloro-3-(dimethylcarbamoyl)phenyl]boronic acid
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