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CAS 850567-23-6

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3-(Cyclopropylaminocarbonyl)phenylboronic acid

Description:
3-(Cyclopropylaminocarbonyl)phenylboronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring, which is further substituted with a cyclopropylaminocarbonyl group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The cyclopropyl group contributes to its unique steric and electronic properties, potentially influencing its reactivity and interaction with biological targets. The presence of the carbonyl group enhances its ability to participate in hydrogen bonding and may affect its solubility and stability in different solvents. Additionally, the compound's structure suggests potential applications in drug development, particularly in the design of inhibitors or modulators of biological pathways. Overall, 3-(Cyclopropylaminocarbonyl)phenylboronic acid is a versatile compound with significant implications in both synthetic and pharmaceutical chemistry.
Formula:C10H12BNO3
InChI:InChI=1/C10H12BNO3/c13-10(12-9-4-5-9)7-2-1-3-8(6-7)11(14)15/h1-3,6,9,14-15H,4-5H2,(H,12,13)
SMILES:c1cc(cc(c1)B(O)O)C(=NC1CC1)O
Synonyms:
  • [3-(Cyclopropylcarbamoyl)phenyl]boronic acid
  • boronic acid, B-[3-[(cyclopropylamino)carbonyl]phenyl]-
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