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CAS 39811-14-8

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6-Chloro-1H-benzimidazole-2-carboxylic acid

Description:
6-Chloro-1H-benzimidazole-2-carboxylic acid is a heterocyclic organic compound characterized by its benzimidazole core, which features a chlorine substituent at the 6-position and a carboxylic acid group at the 2-position. This compound typically appears as a white to off-white solid and is soluble in polar solvents, such as water and alcohols, due to the presence of the carboxylic acid functional group. It exhibits acidic properties, allowing it to participate in various chemical reactions, including esterification and amidation. The chlorine atom introduces unique reactivity and can influence the compound's biological activity, making it of interest in pharmaceutical research. Additionally, the benzimidazole structure is known for its diverse applications, including use as a scaffold in drug development, particularly in anti-parasitic and anti-cancer agents. Overall, 6-Chloro-1H-benzimidazole-2-carboxylic acid is a valuable compound in organic synthesis and medicinal chemistry, with potential implications in various therapeutic areas.
Formula:C8H5ClN2O2
InChI:InChI=1/C8H5ClN2O2/c9-4-1-2-5-6(3-4)11-7(10-5)8(12)13/h1-3H,(H,10,11)(H,12,13)
InChI key:InChIKey=NZIHMSYSZRFUQJ-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1NC=2C(N1)=CC(Cl)=CC2
Synonyms:
  • 1H-Benzimidazole-2-carboxylic acid, 6-chloro-
  • 1H-benzimidazole-2-carboxylic acid, 5-chloro-
  • 2-Benzimidazolecarboxylic acid, 5(or 6)-chloro-
  • 5-Chloro-1H-Benzoimidazole-2-Carboxylic Acid
  • 5-Chlorobenzimidazole-2-carboxylic acid
  • 6-Chloro-1H-benzimidazole-2-carboxylic acid
  • 6-Chlorobenzimidazole-2-carboxylic acid
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