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CAS 874219-19-9

:

B-[4-Fluoro-3-[(methylamino)carbonyl]phenyl]boronic acid

Description:
B-[4-Fluoro-3-[(methylamino)carbonyl]phenyl]boronic acid, with the CAS number 874219-19-9, 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. This compound features a phenyl ring substituted with a fluorine atom and a methylamino carbonyl group, contributing to its unique chemical reactivity and potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. The boronic acid moiety allows for participation in Suzuki coupling reactions, making it valuable in organic synthesis. Additionally, the presence of the fluorine atom can enhance the compound's lipophilicity and metabolic stability, which are important factors in drug design. Its structural characteristics suggest potential interactions with biological targets, making it a candidate for further investigation in therapeutic applications. As with many boronic acids, it may exhibit sensitivity to moisture and should be handled with care in a controlled environment.
Formula:C8H9BFNO3
InChI:InChI=1/C8H9BFNO3/c1-11-8(12)6-4-5(9(13)14)2-3-7(6)10/h2-4,13-14H,1H3,(H,11,12)
InChI key:InChIKey=DVDSMLPVTUSIFM-UHFFFAOYSA-N
SMILES:C(NC)(=O)C1=CC(B(O)O)=CC=C1F
Synonyms:
  • 4-Fluoro-3-(methylaminocarbonyl)benzeneboronic acid
  • 4-Fluoro-3-(methylcarbamoyl)benzeneboronic acid
  • B-[4-fluoro-3-[(methylamino)carbonyl]phenyl]boronic acid
  • Boronic acid, B-[4-fluoro-3-[(methylamino)carbonyl]phenyl]-
  • Boronic acid, [4-fluoro-3-[(methylamino)carbonyl]phenyl]-
  • [4-Fluoro-3-(methylaminocarbonyl)phenyl]boronic acid
  • [4-Fluoro-3-(methylcarbamoyl)phenyl]boronic acid
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