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CAS 850567-39-4

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

Description:
B-[3-[(Dipropylamino)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 organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a dipropylamino group and a carbonyl moiety, which contributes to its chemical reactivity and potential biological activity. Boronic acids are typically polar and can exhibit solubility in polar solvents, while the presence of the dipropylamino group may enhance lipophilicity, influencing its interaction with biological membranes. This compound may also participate in Suzuki-Miyaura cross-coupling reactions, a key method in the formation of carbon-carbon bonds in organic synthesis. Additionally, due to its structural characteristics, it may have applications in drug development, particularly in targeting specific biological pathways or as a tool in chemical biology. As with many boronic acids, careful handling and storage are recommended due to their sensitivity to moisture and air.
Formula:C13H20BNO3
InChI:InChI=1S/C13H20BNO3/c1-3-8-15(9-4-2)13(16)11-6-5-7-12(10-11)14(17)18/h5-7,10,17-18H,3-4,8-9H2,1-2H3
InChI key:InChIKey=FEDZYTLGLQATCT-UHFFFAOYSA-N
SMILES:C(N(CCC)CCC)(=O)C1=CC(B(O)O)=CC=C1
Synonyms:
  • Boronic acid, B-[3-[(dipropylamino)carbonyl]phenyl]-
  • B-[3-[(Dipropylamino)carbonyl]phenyl]boronic acid
  • (3-(Dipropylcarbamoyl)phenyl)boronicacid
  • Boronic acid, [3-[(dipropylamino)carbonyl]phenyl]-
  • (3-(Dipropylcarbamoyl)phenyl)boronic acid
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