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CAS 723282-09-5

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[3-(Isobutylaminocarbonyl)phenyl]boronic acid

Description:
[3-(Isobutylaminocarbonyl)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, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with an isobutylaminocarbonyl group, contributing to its unique reactivity and solubility properties. Typically, boronic acids exhibit moderate solubility in polar solvents and can participate in Suzuki coupling reactions, which are valuable in the formation of carbon-carbon bonds. The presence of the isobutyl group may enhance lipophilicity, potentially influencing the compound's biological activity and interaction with biological targets. Additionally, the compound's structure suggests potential applications in drug development, particularly in the design of inhibitors or modulators of biological pathways. Overall, [3-(Isobutylaminocarbonyl)phenyl]boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C11H16BNO3
InChI:InChI=1/C11H16BNO3/c1-8(2)7-13-11(14)9-4-3-5-10(6-9)12(15)16/h3-6,8,15-16H,7H2,1-2H3,(H,13,14)
SMILES:CC(C)CN=C(c1cccc(c1)B(O)O)O
Synonyms:
  • [3-(Isobutylcarbamoyl)phenyl]boronic acid
  • boronic acid, B-[3-[[(2-methylpropyl)amino]carbonyl]phenyl]-
  • {3-[(2-Methylpropyl)Carbamoyl]Phenyl}Boronic Acid
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