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CAS 2121513-12-8

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B-[3-Chloro-2-(methylthio)phenyl]boronic acid

Description:
B-[3-Chloro-2-(methylthio)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with a chlorine atom and a methylthio 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 chlorine atom and the methylthio group can influence its reactivity and solubility, potentially enhancing its utility in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a common method for forming carbon-carbon bonds. Additionally, boronic acids are known for their role in drug discovery and development, particularly in the design of inhibitors for certain enzymes. The specific structural features of B-[3-Chloro-2-(methylthio)phenyl]boronic acid may also impart unique biological activities, making it a compound of interest in pharmaceutical research.
Formula:C7H8BClO2S
InChI:InChI=1S/C7H8BClO2S/c1-12-7-5(8(10)11)3-2-4-6(7)9/h2-4,10-11H,1H3
InChI key:InChIKey=DCKHSAAPFMPDHL-UHFFFAOYSA-N
SMILES:S(C)C1=C(B(O)O)C=CC=C1Cl
Synonyms:
  • 3-Chloro-2-(methylthio)phenylboronic acid
  • B-[3-Chloro-2-(methylthio)phenyl]boronic acid
  • Boronic acid, B-[3-chloro-2-(methylthio)phenyl]-
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