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CAS 1451392-18-9

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B-[6-Methoxy-4-(methylthio)-3-pyridinyl]boronic acid

Description:
B-[6-Methoxy-4-(methylthio)-3-pyridinyl]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 chemical reactions, particularly in Suzuki coupling reactions. The compound features a pyridine ring substituted with a methoxy group and a methylthio group, which can influence its reactivity and solubility. The methoxy group typically enhances the electron density on the aromatic system, while the methylthio group can provide additional steric and electronic effects. This compound is often utilized in medicinal chemistry and materials science due to its potential applications in drug development and organic synthesis. Its boronic acid functionality also allows for the formation of complexes with biomolecules, making it of interest in biochemical research. Overall, B-[6-Methoxy-4-(methylthio)-3-pyridinyl]boronic acid is a versatile compound with significant implications in both synthetic and biological chemistry.
Formula:C7H10BNO3S
InChI:InChI=1S/C7H10BNO3S/c1-12-7-3-6(13-2)5(4-9-7)8(10)11/h3-4,10-11H,1-2H3
InChI key:InChIKey=GAPDVMBKJLWADV-UHFFFAOYSA-N
SMILES:S(C)C=1C(B(O)O)=CN=C(OC)C1
Synonyms:
  • Boronic acid, B-[6-methoxy-4-(methylthio)-3-pyridinyl]-
  • B-[6-Methoxy-4-(methylthio)-3-pyridinyl]boronic acid
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