4-(Methylthio)phenylboronic acid

For research use only. Not for therapeutic Use.

  • CAT Number: L015296
  • CAS Number: 98546-51-1
  • Molecular Formula: C7H9BO2S
  • Molecular Weight: 168.03
  • Purity: ≥95%
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4-(Methylthio)phenylboronic acid(Cat No.:L015296)is an organoboron compound featuring a methylthio group at the para-position of a phenyl ring bearing a boronic acid functional group. It is commonly used in Suzuki-Miyaura cross-coupling reactions for forming carbon–carbon bonds in the synthesis of biaryl compounds, pharmaceuticals, and advanced organic materials. The electron-donating methylthio group can influence the reactivity and electronic properties of the molecule, enabling selective transformations. Its boronic acid moiety allows for high reactivity under mild conditions, making this compound a versatile and valuable intermediate in modern organic and medicinal chemistry.


CAS Number 98546-51-1
Molecular Formula C7H9BO2S
Purity ≥95%
IUPAC Name (4-methylsulfanylphenyl)boronic acid
InChI InChI=1S/C7H9BO2S/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5,9-10H,1H3
InChIKey IVUHTLFKBDDICS-UHFFFAOYSA-N
SMILES B(C1=CC=C(C=C1)SC)(O)O
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