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CAS 2121513-52-6

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B-[5-Methyl-2-(methylthio)-3-pyridinyl]boronic acid

Description:
B-[5-Methyl-2-(methylthio)-3-pyridinyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. This compound features a methyl group and a methylthio group at specific positions on the pyridine, which can influence its reactivity and solubility. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various applications, including organic synthesis and medicinal chemistry. The presence of the methylthio group may enhance the compound's lipophilicity, potentially affecting its biological activity and interaction with other molecules. Additionally, the compound's structure suggests it may participate in Suzuki-Miyaura cross-coupling reactions, a common method for forming carbon-carbon bonds in organic synthesis. Overall, B-[5-Methyl-2-(methylthio)-3-pyridinyl]boronic acid is a versatile compound with potential applications in drug development and materials science, owing to its unique chemical properties and functional groups.
Formula:C7H10BNO2S
InChI:InChI=1S/C7H10BNO2S/c1-5-3-6(8(10)11)7(12-2)9-4-5/h3-4,10-11H,1-2H3
InChI key:InChIKey=DCZVZGYQNGGQRY-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(SC)N=CC(C)=C1
Synonyms:
  • B-[5-Methyl-2-(methylthio)-3-pyridinyl]boronic acid
  • Boronic acid, B-[5-methyl-2-(methylthio)-3-pyridinyl]-
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