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CAS 874459-90-2

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[4-(2,2,2-trifluoroethylcarbamoyl)phenyl]boronic acid

Description:
[4-(2,2,2-Trifluoroethylcarbamoyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a trifluoroethylcarbamoyl group. This compound typically exhibits properties such as being a solid at room temperature and having moderate solubility in polar solvents due to the presence of both hydrophobic (trifluoroethyl) and hydrophilic (boronic acid) components. The boronic acid moiety allows for potential applications in organic synthesis, particularly in Suzuki coupling reactions, which are valuable in the formation of carbon-carbon bonds. Additionally, the trifluoroethyl group can enhance the compound's lipophilicity and stability, making it useful in medicinal chemistry and material science. The presence of the carbamoyl group may also impart specific biological activities or interactions, making this compound of interest in drug development and biochemical research. Overall, its unique structural features contribute to its versatility in various chemical applications.
Formula:C9H9BF3NO3
InChI:InChI=1/C9H9BF3NO3/c11-9(12,13)5-14-8(15)6-1-3-7(4-2-6)10(16)17/h1-4,16-17H,5H2,(H,14,15)
SMILES:c1cc(ccc1C(=O)NCC(F)(F)F)B(O)O
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