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CAS 1451392-52-1

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

Description:
B-[3-Chloro-5-(methylthio)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 valuable in various chemical reactions, particularly in Suzuki coupling reactions. The compound features a chlorinated aromatic ring, which enhances its reactivity and potential applications in medicinal chemistry and material science. The methylthio group contributes to its electronic properties and solubility characteristics. Typically, boronic acids like this one are utilized in organic synthesis, particularly for the construction of complex molecules in pharmaceuticals and agrochemicals. Additionally, the presence of the chlorine and methylthio substituents can influence the compound's biological activity and interaction with other molecules. Overall, B-[3-Chloro-5-(methylthio)phenyl]boronic acid is a versatile building block in synthetic organic chemistry, with potential applications in drug development and materials science.
Formula:C7H8BClO2S
InChI:InChI=1S/C7H8BClO2S/c1-12-7-3-5(8(10)11)2-6(9)4-7/h2-4,10-11H,1H3
InChI key:InChIKey=GQYXPJXCFHHTIF-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(SC)=CC(Cl)=C1
Synonyms:
  • B-[3-Chloro-5-(methylthio)phenyl]boronic acid
  • Boronic acid, B-[3-chloro-5-(methylthio)phenyl]-
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