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CAS 874289-48-2

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B-[2-Fluoro-5-[(propylamino)carbonyl]phenyl]boronic acid

Description:
B-[2-Fluoro-5-[(propylamino)carbonyl]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, making it useful in various applications, including medicinal chemistry and materials science. The compound features a fluorinated phenyl ring, which can enhance its biological activity and solubility properties. The propylamino substituent contributes to its potential as a ligand in drug design, particularly in the development of inhibitors for specific biological targets. The boronic acid moiety allows for participation in Suzuki coupling reactions, a key method in organic synthesis for forming carbon-carbon bonds. Additionally, the presence of the fluorine atom may influence the electronic properties and reactivity of the compound. Overall, this substance is of interest in both synthetic chemistry and pharmaceutical research due to its unique structural features and functional capabilities.
Formula:C10H13BFNO3
InChI:InChI=1S/C10H13BFNO3/c1-2-5-13-10(14)7-3-4-9(12)8(6-7)11(15)16/h3-4,6,15-16H,2,5H2,1H3,(H,13,14)
InChI key:InChIKey=UTFWGDUSGXDUNF-UHFFFAOYSA-N
SMILES:C(NCCC)(=O)C1=CC(B(O)O)=C(F)C=C1
Synonyms:
  • [2-Fluoro-5-(propylcarbamoyl)phenyl]boronic acid
  • (2-Fluoro-5-(propylcarbamoyl)phenyl)boronicacid
  • B-[2-Fluoro-5-[(propylamino)carbonyl]phenyl]boronic acid
  • Boronic acid, [2-fluoro-5-[(propylamino)carbonyl]phenyl]-
  • Boronic acid, B-[2-fluoro-5-[(propylamino)carbonyl]phenyl]-
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