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CAS 129112-21-6

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2-(N,N-DIETHYLAMINOCARBONYL)PHENYLBORONIC ACID

Description:
2-(N,N-Diethylaminocarbonyl)phenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring, which is further substituted with a diethylaminocarbonyl group. This compound typically exhibits properties such as moderate solubility in polar organic solvents and potential reactivity in various chemical transformations, particularly in Suzuki-Miyaura cross-coupling reactions, where boronic acids are utilized as coupling partners. The presence of the diethylamino group can enhance its nucleophilicity and influence its electronic properties, making it useful in organic synthesis and medicinal chemistry. Additionally, boronic acids are known for their ability to form reversible covalent bonds with diols, which can be exploited in sensor applications and drug delivery systems. The compound's structure suggests it may also exhibit interesting biological activity, although specific biological properties would require further investigation. Overall, 2-(N,N-Diethylaminocarbonyl)phenylboronic acid is a versatile compound with potential applications in various fields of chemistry.
Formula:C11H16BNO3
InChI:InChI=1/C11H16BNO3/c1-3-13(4-2)11(14)9-7-5-6-8-10(9)12(15)16/h5-8,15-16H,3-4H2,1-2H3
SMILES:CCN(CC)C(=O)c1ccccc1B(O)O
Synonyms:
  • 2-[(Diethylamino)Carbonyl]Benzeneboronic Acid
  • 2-(N,N-Diethylcarbamoyl)Phenylboronic Acid
  • Rarechem Ah Pb 0055
  • N,N-Diethyl 4-Boronobenzamide
  • 2-(Diethylcarbamoyl)benzeneboronic acid
  • 2-(Diethylcarbamoyl)benzeneboronic acid 95%
  • [2-(Diethylcarbamoyl)Phenyl]Boronic Acid
  • (2-(Diethylcarbamoyl)phenyl)boronicacid
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