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CAS 480424-55-3

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

Description:
(3-formyl-2-methoxy-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, including organic synthesis and medicinal chemistry. This compound features a phenyl ring substituted with a formyl group, a methoxy group, and a methyl group, contributing to its unique reactivity and solubility properties. The presence of the formyl group indicates potential for further functionalization, while the methoxy and methyl groups can influence the electronic properties and steric hindrance of the molecule. Typically, boronic acids like this one are utilized in Suzuki coupling reactions, which are essential for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the compound may exhibit interesting biological activities due to its structural features, making it a candidate for research in drug development and materials science. Overall, its distinctive functional groups and boronic acid moiety make it a valuable compound in synthetic organic chemistry.
Formula:C9H11BO4
InChI:InChI=1/C9H11BO4/c1-6-3-7(5-11)9(14-2)8(4-6)10(12)13/h3-5,12-13H,1-2H3
SMILES:Cc1cc(C=O)c(c(c1)B(O)O)OC
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