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CAS 138642-97-4

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6-Chloroimidazo[1,2-a]pyridine-3-carboxylic acid

Description:
6-Chloroimidazo[1,2-a]pyridine-3-carboxylic acid is a heterocyclic compound characterized by its imidazo and pyridine rings, which contribute to its unique chemical properties. The presence of a chlorine atom at the 6-position of the imidazo ring enhances its reactivity and potential for forming various derivatives. The carboxylic acid functional group at the 3-position is significant for its acidity and ability to participate in hydrogen bonding, making it a useful building block in organic synthesis and medicinal chemistry. This compound is often studied for its biological activity, particularly in the context of drug development, as it may exhibit antimicrobial or anticancer properties. Its solubility and stability in various solvents can vary, influencing its application in different chemical reactions. Additionally, the compound's molecular structure allows for potential interactions with biological targets, making it a subject of interest in pharmacological research. Overall, 6-Chloroimidazo[1,2-a]pyridine-3-carboxylic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C8H5ClN2O2
InChI:InChI=1S/C8H5ClN2O2/c9-5-1-2-7-10-3-6(8(12)13)11(7)4-5/h1-4H,(H,12,13)
InChI key:InChIKey=LXRDUEDQFSBROM-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1N2C(=NC1)C=CC(Cl)=C2
Synonyms:
  • Imidazo[1,2-a]pyridine-3-carboxylic acid, 6-chloro-
  • 6-Chloroimidazo[1,2-a]pyridine-3-carboxylic acid
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