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CAS 874288-34-3

:

[3-[(3-fluorophenyl)carbamoyl]phenyl]boronic acid

Description:
[3-[(3-fluorophenyl)carbamoyl]phenyl]boronic acid, with the CAS number 874288-34-3, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and a carbamoyl substituent. 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 fluorophenyl group may enhance its biological activity and solubility in organic solvents. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are vital for constructing complex organic molecules. The compound's structure suggests potential applications in drug development, particularly in targeting specific biological pathways due to its ability to interact with biomolecules. Overall, [3-[(3-fluorophenyl)carbamoyl]phenyl]boronic acid is a versatile compound with significant implications in both synthetic and pharmaceutical chemistry.
Formula:C13H11BFNO3
InChI:InChI=1/C13H11BFNO3/c15-11-5-2-6-12(8-11)16-13(17)9-3-1-4-10(7-9)14(18)19/h1-8,18-19H,(H,16,17)
SMILES:c1cc(cc(c1)B(O)O)C(=Nc1cccc(c1)F)O
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