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CAS 237413-05-7

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3-(N,N-Diethylaminocarbonyl)phenylboronic acid

Description:
3-(N,N-Diethylaminocarbonyl)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 diethylaminocarbonyl group. This compound typically exhibits properties associated with both boronic acids and amides, including the ability to form reversible covalent bonds with diols, making it useful in various applications such as organic synthesis and medicinal chemistry. The presence of the diethylamino group enhances its solubility in organic solvents and may influence its reactivity and interaction with biological systems. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. The compound's structure suggests potential applications in drug development and materials science, particularly in the design of sensors or catalysts. As with many boronic acids, it may exhibit pH-dependent behavior, affecting its reactivity and stability in different environments.
Formula:C11H16BNO3
InChI:InChI=1/C11H16BNO3/c1-3-13(4-2)11(14)9-6-5-7-10(8-9)12(15)16/h5-8,15-16H,3-4H2,1-2H3
SMILES:CCN(CC)C(=O)c1cccc(c1)B(O)O
Synonyms:
  • (3-(Diethylcarbamoyl)phenyl)boronicacid
  • [3-(Diethylcarbamoyl)Phenyl]Boronic Acid
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