CAS 913835-66-2
:(5-methylsulfanyl-3-pyridyl)sulfanylmethylboronic acid
Description:
(5-Methylsulfanyl-3-pyridyl)sulfanylmethylboronic acid is a boronic acid derivative characterized by the presence of a pyridine ring substituted with a methylsulfanyl group and a sulfanylmethyl group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the pyridine ring contributes to its potential as a ligand in coordination chemistry and its role in biological systems. Additionally, the functional groups present in this compound may influence its solubility, reactivity, and interaction with biological targets. As a boronic acid, it may also participate in Suzuki coupling reactions, which are valuable in the formation of carbon-carbon bonds. Overall, this compound's unique structure and functional groups make it a subject of interest in both synthetic and pharmaceutical chemistry.
Formula:C7H10BNO2S2
InChI:InChI=1/C7H10BNO2S2/c1-12-6-2-7(4-9-3-6)13-5-8(10)11/h2-4,10-11H,5H2,1H3
SMILES:CSc1cc(cnc1)SCB(O)O
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Found 2 products.
5-(Methylthio)pyridin-3-ylthiomethylboronic acid
CAS:<p>5-(Methylthio)pyridin-3-ylthiomethylboronic acid</p>Purity:95%Molecular weight:215.10g/mol
