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CAS 874289-11-9

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[4-(cyclohexylcarbamoyl)-3-fluoro-phenyl]boronic acid

Description:
[4-(Cyclohexylcarbamoyl)-3-fluoro-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 and play a crucial role in Suzuki coupling reactions. This compound features a phenyl ring substituted with a cyclohexylcarbamoyl group and a fluorine atom, which can influence its reactivity and solubility. The cyclohexylcarbamoyl moiety may enhance the compound's lipophilicity, potentially affecting its biological activity and interaction with various targets. The presence of the fluorine atom can also modify the electronic properties of the molecule, impacting its stability and reactivity. As a boronic acid, it can participate in various chemical transformations, making it valuable in organic synthesis and medicinal chemistry. Its specific applications may include use in drug development, particularly in the synthesis of biologically active compounds or as a building block in complex organic molecules.
Formula:C13H17BFNO3
InChI:InChI=1/C13H17BFNO3/c15-12-8-9(14(18)19)6-7-11(12)13(17)16-10-4-2-1-3-5-10/h6-8,10,18-19H,1-5H2,(H,16,17)
SMILES:C1CCC(CC1)N=C(c1ccc(cc1F)B(O)O)O
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