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CAS 123088-59-5

:

[4-(Aminocarbonyl)phenyl]-boronic acid

Description:
[4-(Aminocarbonyl)phenyl]-boronic acid, with the CAS number 123088-59-5, is an organic compound that features a boronic acid functional group attached to a phenyl ring that also contains an aminocarbonyl substituent. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the boronic acid group, which can form hydrogen bonds. The aminocarbonyl group contributes to its potential reactivity, making it useful in various chemical reactions, including Suzuki coupling reactions, which are important in organic synthesis for forming carbon-carbon bonds. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications and drug delivery systems. The compound's structure allows it to participate in diverse chemical transformations, making it valuable in medicinal chemistry and materials science. Its properties and reactivity are influenced by the electronic effects of both the boronic acid and the aminocarbonyl groups.
Formula:C7H8BNO3
InChI:InChI=1/C7H8BNO3/c9-7(10)5-1-3-6(4-2-5)8(11)12/h1-4,11-12H,(H2,9,10)
SMILES:c1cc(ccc1C(=O)N)B(O)O
Synonyms:
  • (4-Aminocarbonylphenyl)boronic acid
  • (4-Carbamoylphenyl)Boronic Acid
  • 4-Carbamoylphenylboronicacid
  • 4-Aminocarbonylphenylboronic acid
  • 4-(Aminocarbonyl)Benzeneboronic Acid
  • 4-Carbamoylphenylboronic acid
  • 4-Aminocarbonylphenylboronic acid ,98%
  • 4-CARBOXAMIDEPHENYLBORONIC ACID
  • P-(AMINOCARBONYL)PHENYLBORONIC ACID
  • 4-(Aminocarbonyl)Phenylboronic
  • BENZAMIDE-4-BORONIC ACID
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