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CAS 1218790-68-1

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B-[2-(2-Methylpropoxy)-5-(trifluoromethyl)-3-pyridinyl]boronic acid

Description:
B-[2-(2-Methylpropoxy)-5-(trifluoromethyl)-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 and other nucleophiles. This compound features a pyridine ring substituted with a trifluoromethyl group, enhancing its electronic properties and potentially increasing its lipophilicity. The presence of the 2-methylpropoxy group contributes to its solubility and stability in various solvents. Boronic acids are often utilized in organic synthesis, particularly in Suzuki coupling reactions, which are pivotal for forming carbon-carbon bonds. Additionally, this compound may exhibit biological activity, making it of interest in medicinal chemistry. Its unique structural features, including the trifluoromethyl and alkoxy substituents, suggest potential applications in pharmaceuticals or agrochemicals. As with many boronic acids, careful handling and storage are essential due to their sensitivity to moisture and air, which can lead to hydrolysis and loss of reactivity.
Formula:C10H13BF3NO3
InChI:InChI=1S/C10H13BF3NO3/c1-6(2)5-18-9-8(11(16)17)3-7(4-15-9)10(12,13)14/h3-4,6,16-17H,5H2,1-2H3
InChI key:InChIKey=XNIVHYIBMDZMCA-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(OCC(C)C)N=CC(C(F)(F)F)=C1
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