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CAS 874288-05-8

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[4-[(3-fluorophenyl)carbamoyl]phenyl]boronic acid

Description:
[4-[(3-fluorophenyl)carbamoyl]phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols and is widely used in organic synthesis and medicinal chemistry. This compound features a phenyl ring substituted with a carbamoyl group and a fluorophenyl moiety, contributing to its potential biological activity and specificity in various applications. The fluorine atom in the structure can enhance the compound's lipophilicity and influence its interaction with biological targets. As a boronic acid, it can participate in Suzuki coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the compound's solubility and stability in different solvents can vary, which is important for its practical applications in research and industry. Overall, [4-[(3-fluorophenyl)carbamoyl]phenyl]boronic acid represents a versatile building block in the field of organic chemistry and drug development.
Formula:C13H11BFNO3
InChI:InChI=1/C13H11BFNO3/c15-11-2-1-3-12(8-11)16-13(17)9-4-6-10(7-5-9)14(18)19/h1-8,18-19H,(H,16,17)
SMILES:c1cc(cc(c1)NC(=O)c1ccc(cc1)B(O)O)F
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