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CAS 252663-47-1

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4-(N-Benzylaminocarbonyl)phenylboronic acid

Description:
4-(N-Benzylaminocarbonyl)phenylboronic 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 valuable in various chemical reactions, particularly in Suzuki coupling reactions. This compound features a phenyl ring substituted with a benzylaminocarbonyl group, enhancing its solubility and reactivity. The boronic acid moiety contributes to its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals and agrochemicals. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents. Its reactivity can be influenced by the presence of the carbonyl group, which can participate in hydrogen bonding and affect the overall electronic properties of the molecule. Additionally, the compound's structure allows for potential interactions with biological targets, making it a subject of interest in drug design and development. Safety and handling precautions should be observed due to the potential reactivity of boronic acids.
Formula:C14H14BNO3
InChI:InChI=1/C14H14BNO3/c17-14(16-10-11-4-2-1-3-5-11)12-6-8-13(9-7-12)15(18)19/h1-9,18-19H,10H2,(H,16,17)
SMILES:c1ccc(cc1)CNC(=O)c1ccc(cc1)B(O)O
Synonyms:
  • [4-(Benzylcarbamoyl)Phenyl]Boronic Acid
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