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CAS 874219-24-6

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

Description:
[3-(Cyclohexylcarbamoyl)-4-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 other nucleophiles. This compound features a phenyl ring substituted with a fluorine atom and a cyclohexylcarbamoyl group, which contributes to its unique chemical properties. The presence of the boronic acid moiety allows it to participate in various chemical reactions, including Suzuki coupling, making it valuable in organic synthesis and medicinal chemistry. Its structural features may influence its solubility, reactivity, and potential biological activity. Additionally, the cyclohexyl group can enhance lipophilicity, potentially affecting the compound's pharmacokinetics. Overall, this compound's characteristics make it a subject of interest in research areas such as drug development and materials science, particularly in the context of developing new therapeutic agents or functional materials.
Formula:C13H17BFNO3
InChI:InChI=1/C13H17BFNO3/c15-12-7-6-9(14(18)19)8-11(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(c1cc(ccc1F)B(O)O)O
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