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CAS 477251-98-2

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5-(Methylthio)pyridine-3-boronic acid

Description:
5-(Methylthio)pyridine-3-boronic acid is an organoboron compound characterized by the presence of a pyridine ring substituted with a methylthio group and a boronic acid functional group. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, which is a common trait for boronic acids due to their ability to form hydrogen bonds. The methylthio group enhances its reactivity and can participate in various chemical reactions, including Suzuki coupling, which is significant in organic synthesis and medicinal chemistry. The boronic acid moiety allows for the formation of reversible complexes with diols, making it useful in the development of sensors and in drug delivery systems. Additionally, this compound may exhibit biological activity, which can be explored in pharmaceutical applications. Overall, 5-(Methylthio)pyridine-3-boronic acid serves as a versatile building block in synthetic organic chemistry and has potential applications in various fields, including materials science and biochemistry.
Formula:C6H8BNO2S
InChI:InChI=1/C6H8BNO2S/c1-11-6-2-5(7(9)10)3-8-4-6/h2-4,9-10H,1H3
SMILES:CSc1cc(cnc1)B(O)O
Synonyms:
  • [5-(Methylsulfanyl)pyridin-3-yl]boronic acid
  • boronic acid, B-[5-(methylthio)-3-pyridinyl]-
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