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CAS 1451390-91-2

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B-[2-Methyl-6-(2-methylpropoxy)-3-pyridinyl]boronic acid

Description:
B-[2-Methyl-6-(2-methylpropoxy)-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 methyl group and a branched alkoxy group, contributing to its unique chemical properties. The boronic acid moiety allows for potential applications in medicinal chemistry, particularly in drug development and as a building block in organic synthesis. Its structure suggests it may exhibit specific reactivity patterns, including participation in Suzuki coupling reactions, which are valuable in forming carbon-carbon bonds. Additionally, the presence of the alkoxy group may influence its solubility and stability in various solvents. Overall, this compound's characteristics make it a subject of interest in both academic research and industrial applications, particularly in the fields of organic synthesis and materials science.
Formula:C10H16BNO3
InChI:InChI=1S/C10H16BNO3/c1-7(2)6-15-10-5-4-9(11(13)14)8(3)12-10/h4-5,7,13-14H,6H2,1-3H3
InChI key:InChIKey=UXVYTZHMEMUJIW-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(C)N=C(OCC(C)C)C=C1
Synonyms:
  • B-[2-Methyl-6-(2-methylpropoxy)-3-pyridinyl]boronic acid
  • Boronic acid, B-[2-methyl-6-(2-methylpropoxy)-3-pyridinyl]-
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