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CAS 850567-22-5

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B-[3-[(Propylamino)carbonyl]phenyl]boronic acid

Description:
B-[3-[(Propylamino)carbonyl]phenyl]boronic acid is an organic 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 propylamino group and a carbonyl moiety, contributing to its potential reactivity and solubility properties. The boronic acid functionality allows it to participate in various chemical reactions, including Suzuki coupling, making it valuable in organic synthesis and medicinal chemistry. Additionally, the presence of the propylamino group may enhance its biological activity and solubility in organic solvents. The compound's structure suggests potential applications in drug development, particularly in targeting specific biological pathways or as a building block for more complex molecules. Its unique characteristics, including its ability to interact with biomolecules, make it a subject of interest in research related to pharmaceuticals and materials science.
Formula:C10H14BNO3
InChI:InChI=1S/C10H14BNO3/c1-2-6-12-10(13)8-4-3-5-9(7-8)11(14)15/h3-5,7,14-15H,2,6H2,1H3,(H,12,13)
InChI key:InChIKey=DZGOREURDIPFFZ-UHFFFAOYSA-N
SMILES:C(NCCC)(=O)C1=CC(B(O)O)=CC=C1
Synonyms:
  • 3-(N-Propylaminocarbonyl)phenylboronic acid
  • 3-(Propylcarbamoyl)phenylboronic acid
  • B-[3-[(Propylamino)carbonyl]phenyl]boronic acid
  • Boronic acid, B-[3-[(propylamino)carbonyl]phenyl]-
  • Boronic acid, [3-[(propylamino)carbonyl]phenyl]-
  • [3-(N-Propylaminocarbonyl)phenyl]boronic acid
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