CAS 874219-41-7
:[3-(benzylcarbamoyl)-5-fluoro-phenyl]boronic acid
Description:
[3-(Benzylcarbamoyl)-5-fluoro-phenyl]boronic acid is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl ring that is substituted with both a benzylcarbamoyl group and a fluorine atom. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the fluorine atom can enhance the compound's lipophilicity and influence its biological activity. Additionally, the benzylcarbamoyl moiety may contribute to the compound's solubility and reactivity. As a boronic acid, it may also participate in Suzuki coupling reactions, which are valuable in the formation of carbon-carbon bonds. Overall, this compound's unique structural features make it a candidate for further research in drug development and materials science.
Formula:C14H13BFNO3
InChI:InChI=1/C14H13BFNO3/c16-13-7-11(6-12(8-13)15(19)20)14(18)17-9-10-4-2-1-3-5-10/h1-8,19-20H,9H2,(H,17,18)
SMILES:c1ccc(cc1)CN=C(c1cc(cc(c1)F)B(O)O)O
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Found 3 products.
3-(Benzylcarbamoyl)-5-fluorobenzeneboronic acid
CAS:Formula:C14H13BFNO3Purity:95%Color and Shape:SolidMolecular weight:273.06733-(Benzylcarbamoyl)-5-fluorobenzeneboronic acid
CAS:<p>3-(Benzylcarbamoyl)-5-fluorobenzeneboronic acid</p>Purity:98%Molecular weight:273.07g/mol(3-(Benzylcarbamoyl)-5-fluorophenyl)boronic acid
CAS:Formula:C14H13BFNO3Purity:≥95%Molecular weight:273.07


