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CAS 174422-14-1

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2-(4-Chlorophenyl)-1H-benzimidazole-6-carboxylic acid

Description:
2-(4-Chlorophenyl)-1H-benzimidazole-6-carboxylic acid is a chemical compound characterized by its benzimidazole core, which is a bicyclic structure containing both benzene and imidazole rings. The presence of a 4-chlorophenyl group indicates that a chlorine atom is substituted on the phenyl ring at the para position, contributing to the compound's unique electronic and steric properties. The carboxylic acid functional group at the 6-position of the benzimidazole enhances its acidity and reactivity, making it suitable for various chemical reactions and applications. This compound is often studied for its potential biological activities, including antimicrobial and anticancer properties, due to the structural features that can interact with biological targets. Additionally, its solubility and stability in different solvents can vary, influencing its practical applications in pharmaceuticals and research. Overall, 2-(4-Chlorophenyl)-1H-benzimidazole-6-carboxylic acid is a significant compound in medicinal chemistry, with ongoing research into its properties and potential uses.
Formula:C14H9ClN2O2
InChI:InChI=1S/C14H9ClN2O2/c15-10-4-1-8(2-5-10)13-16-11-6-3-9(14(18)19)7-12(11)17-13/h1-7H,(H,16,17)(H,18,19)
InChI key:InChIKey=KFEDCUOAVSSAAS-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1C=C2C(N=C(N2)C3=CC=C(Cl)C=C3)=CC1
Synonyms:
  • 2-(4-Chlorophenyl)-1H-1,3-benzodiazole-5-carboxylic acid
  • 2-(4-Chlorophenyl)-1H-benzimidazole-6-carboxylic acid
  • 1H-Benzimidazole-6-carboxylic acid, 2-(4-chlorophenyl)-
  • AC 271251
  • 1H-Benzimidazole-5-carboxylic acid, 2-(4-chlorophenyl)-
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