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CAS 871332-63-7

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[3-fluoro-5-(methylcarbamoyl)phenyl]boronic acid

Description:
[3-Fluoro-5-(methylcarbamoyl)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 is widely used in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a fluorine atom and a methylcarbamoyl group, which contributes to its unique reactivity and potential biological activity. The fluorine substitution can enhance the lipophilicity and metabolic stability of the compound, while the boronic acid moiety allows for participation in Suzuki coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the methylcarbamoyl group may impart specific pharmacological properties, potentially influencing the compound's interaction with biological targets. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their applications in drug development and material science.
Formula:C8H9BFNO3
InChI:InChI=1/C8H9BFNO3/c1-11-8(12)5-2-6(9(13)14)4-7(10)3-5/h2-4,13-14H,1H3,(H,11,12)
SMILES:CN=C(c1cc(cc(c1)F)B(O)O)O
Synonyms:
  • boronic acid, B-[3-fluoro-5-[(methylamino)carbonyl]phenyl]-
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