CAS 628692-16-0
:(2-methylquinolin-5-yl)boronic acid
Description:
(2-Methylquinolin-5-yl)boronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a quinoline ring system. This compound features a methyl group at the 2-position of the quinoline, which contributes to its unique chemical properties. 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 quinoline moiety may impart biological activity, as quinolines are often found in pharmaceuticals and agrochemicals. The compound is typically a solid at room temperature and may exhibit solubility in polar organic solvents. Its reactivity can be influenced by the boronic acid group, allowing for participation in cross-coupling reactions, which are essential in the formation of carbon-carbon bonds. Overall, (2-methylquinolin-5-yl)boronic acid is a versatile building block in synthetic chemistry, with potential applications in drug development and material science.
Formula:C10H10BNO2
InChI:InChI=1/C10H10BNO2/c1-7-5-6-8-9(11(13)14)3-2-4-10(8)12-7/h2-6,13-14H,1H3
SMILES:Cc1ccc2c(cccc2n1)B(O)O
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Found 4 products.
(2-Methylquinolin-5-yl)boronic acid
CAS:Formula:C10H10BNO2Purity:95%Color and Shape:SolidMolecular weight:187.0029(2-Methylquinolin-5-yl)boronic acid
CAS:(2-Methylquinolin-5-yl)boronic acidPurity:98%Molecular weight:187.01g/mol(2-methylquinolin-5-yl)boronic acid hydrate
CAS:Formula:C10H12BNO3Purity:95.0%Molecular weight:205.02



