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CAS 850568-15-9

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[4-(cyclopentylcarbamoyl)phenyl]boronic acid

Description:
[4-(Cyclopentylcarbamoyl)phenyl]boronic 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 a cyclopentylcarbamoyl group. This compound typically exhibits properties common to 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 cyclopentylcarbamoyl moiety may enhance its solubility and biological activity, potentially influencing its interactions in biological systems. The compound is likely to be a white to off-white solid, with moderate solubility in polar solvents. Its reactivity is characterized by the ability to participate in Suzuki-Miyaura cross-coupling reactions, which are valuable in the formation of carbon-carbon bonds. Additionally, the presence of the boronic acid group allows for potential applications in drug development, particularly in the design of inhibitors for certain enzymes or receptors. Overall, [4-(cyclopentylcarbamoyl)phenyl]boronic acid represents a versatile building block in synthetic organic chemistry.
Formula:C12H16BNO3
InChI:InChI=1/C12H16BNO3/c15-12(14-11-3-1-2-4-11)9-5-7-10(8-6-9)13(16)17/h5-8,11,16-17H,1-4H2,(H,14,15)
SMILES:C1CCC(C1)NC(=O)c1ccc(cc1)B(O)O
Synonyms:
  • Boronic acid, B-[4-[(cyclopentylamino)carbonyl]phenyl]-
  • [4-(Cyclopentylcarbamoyl)phenyl]boronic acid
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