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CAS 480424-51-9

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(2-butoxy-3-formyl-5-methylphenyl)boronic acid

Description:
(2-butoxy-3-formyl-5-methylphenyl)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, making it useful in various applications, particularly in organic synthesis and medicinal chemistry. This compound features a phenyl ring substituted with a butoxy group, a formyl group, and a methyl group, contributing to its unique reactivity and solubility properties. The presence of the boronic acid moiety allows for participation in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. Additionally, the structural features of this compound may influence its biological activity, making it a candidate for further investigation in drug development. Its solubility in organic solvents and stability under various conditions are also important characteristics that facilitate its use in synthetic pathways. Overall, (2-butoxy-3-formyl-5-methylphenyl)boronic acid exemplifies the versatility of boronic acids in modern chemistry.
Formula:C12H17BO4
InChI:InChI=1/C12H17BO4/c1-3-4-5-17-12-10(8-14)6-9(2)7-11(12)13(15)16/h6-8,15-16H,3-5H2,1-2H3
SMILES:CCCCOc1c(cc(C)cc1B(O)O)C=O
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