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CAS 397843-69-5

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3-(N-Isopropylaminocarbonyl)phenylboronic acid

Description:
3-(N-Isopropylaminocarbonyl)phenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with an isopropylaminocarbonyl group. This compound typically exhibits properties such as moderate solubility in polar solvents due to the presence of the boronic acid moiety, which can engage in hydrogen bonding and coordination with other molecules. The boronic acid group is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including drug development and materials science. The isopropylaminocarbonyl substituent may influence the compound's reactivity and biological activity, potentially enhancing its interaction with biological targets. Additionally, the compound's structure suggests it may participate in Suzuki-Miyaura cross-coupling reactions, a key method in organic synthesis for forming carbon-carbon bonds. Overall, 3-(N-Isopropylaminocarbonyl)phenylboronic acid is a versatile compound with potential applications in medicinal chemistry and organic synthesis.
Formula:C10H14BNO3
InChI:InChI=1/C10H14BNO3/c1-7(2)12-10(13)8-4-3-5-9(6-8)11(14)15/h3-7,14-15H,1-2H3,(H,12,13)
SMILES:CC(C)N=C(c1cccc(c1)B(O)O)O
Synonyms:
  • {3-[(1-Methylethyl)Carbamoyl]Phenyl}Boronic Acid
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