CAS 254893-03-3
:[4-(3-oxocyclobutyl)phenyl]boronic acid
Description:
[4-(3-Oxocyclobutyl)phenyl]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. This compound features a phenyl ring substituted with a cyclobutyl moiety that contains a ketone functional group, contributing to its unique reactivity and potential applications in organic synthesis and medicinal chemistry. The boronic acid group allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the formation of carbon-carbon bonds. Additionally, the presence of the cyclobutyl group may influence the compound's steric and electronic properties, potentially affecting its reactivity and interactions with biological targets. As with many boronic acids, it is likely to exhibit moderate solubility in polar solvents and may be sensitive to moisture, requiring careful handling and storage conditions. Overall, this compound's structural features suggest it could be of interest in the development of new materials or pharmaceuticals.
Formula:C10H11BO3
InChI:InChI=1/C10H11BO3/c12-10-5-8(6-10)7-1-3-9(4-2-7)11(13)14/h1-4,8,13-14H,5-6H2
SMILES:c1cc(ccc1C1CC(=O)C1)B(O)O
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Found 3 products.
3-(4-Boronophenyl)cyclobutanone
CAS:3-(4-Boronophenyl)cyclobutanonePurity:≥95%Molecular weight:190.00g/mol


