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CAS 871332-65-9

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[4-Chloro-3-(methylcarbamoyl)phenyl]boronic acid

Description:
[4-Chloro-3-(methylcarbamoyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a chlorinated phenyl ring, which can influence its reactivity and solubility, as well as a methylcarbamoyl group that may enhance its biological activity. Typically, boronic acids exhibit moderate to high solubility in polar solvents, and their acidity can be attributed to the boron atom's ability to donate a proton. This compound may also participate in Suzuki-Miyaura cross-coupling reactions, a key method in the formation of carbon-carbon bonds. Additionally, the presence of the methylcarbamoyl group suggests potential interactions with biological targets, making it of interest in drug discovery. Overall, [4-Chloro-3-(methylcarbamoyl)phenyl]boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C8H9BClNO3
InChI:InChI=1/C8H9BClNO3/c1-11-8(12)6-4-5(9(13)14)2-3-7(6)10/h2-4,13-14H,1H3,(H,11,12)
SMILES:CN=C(c1cc(ccc1Cl)B(O)O)O
Synonyms:
  • boronic acid, B-[4-chloro-3-[(methylamino)carbonyl]phenyl]-
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