CAS 480424-63-3
:(4-ethoxy-3-formylphenyl)boronic acid
Description:
(4-Ethoxy-3-formylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that also features an ethoxy and a formyl substituent. This compound typically exhibits properties such as moderate solubility in organic solvents and potential reactivity with various electrophiles due to the boronic acid moiety, which can participate in Suzuki coupling reactions. The presence of the formyl group suggests that it can undergo further transformations, such as reduction or condensation reactions. Additionally, the ethoxy group may influence the compound's polarity and solubility, making it useful in organic synthesis and medicinal chemistry. The boronic acid functionality is particularly valuable in the development of pharmaceuticals and agrochemicals, as it can form reversible complexes with diols and other Lewis bases. Overall, (4-ethoxy-3-formylphenyl)boronic acid is a versatile compound with applications in synthetic organic chemistry and materials science.
Formula:C9H11BO4
InChI:InChI=1/C9H11BO4/c1-2-14-9-4-3-8(10(12)13)5-7(9)6-11/h3-6,12-13H,2H2,1H3
SMILES:CCOc1ccc(cc1C=O)B(O)O
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Found 3 products.
(4-Ethoxy-3-formylphenyl)boronic acid
CAS:Formula:C9H11BO4Purity:98%Color and Shape:SolidMolecular weight:193.99223-Formyl-4-ethoxyphenylboronic acid
CAS:<p>3-Formyl-4-ethoxyphenylboronic acid</p>Purity:≥95%Molecular weight:193.99g/mol


