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CAS 168618-42-6

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2-Methylsulfanylphenylboronic acid

Description:
2-Methylsulfanylphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that also features a methylthio substituent. This compound typically exhibits properties common to 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 methylthio group can influence the compound's reactivity and solubility, potentially enhancing its biological activity or selectivity in chemical reactions. In terms of physical properties, boronic acids often have moderate solubility in polar solvents and can exist in different tautomeric forms. The presence of the boron atom allows for coordination with other molecules, which is significant in the context of drug design and materials science. Overall, 2-Methylsulfanylphenylboronic acid is a versatile compound with potential applications in catalysis, sensor development, and as a building block in the synthesis of more complex organic molecules.
Formula:C7H9BO2S
InChI:InChI=1S/C7H9BO2S/c1-11-7-5-3-2-4-6(7)8(9)10/h2-5,9-10H,1H3
InChI key:InChIKey=QXBWTYBCNFKURT-UHFFFAOYSA-N
SMILES:S(C)C1=C(B(O)O)C=CC=C1
Synonyms:
  • 2-(Methylmercapto)-Phenylboronic Acid
  • 2-(Methylthio)benzeneboronic acid
  • 2-(Methylthio)phenylboronic acid
  • 2-Boronothioanisole
  • 2-Methylsulfanylphenylboronic acid
  • 2-Methylthiophenylboronic acid
  • 2-Thioanisoleboronic acid
  • B-[2-(Methylthio)phenyl]boronic acid
  • Boronic acid, B-[2-(methylthio)phenyl]-
  • Boronic acid, [2-(methylthio)phenyl]-
  • [2-(Methylthio)phenyl]boronic acid
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