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CAS 117390-36-0

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5-Chlorothieno[3,2-b]pyridine-6-carboxylic acid

Description:
5-Chlorothieno[3,2-b]pyridine-6-carboxylic acid is a heterocyclic compound characterized by its unique structure, which includes a thieno[3,2-b]pyridine ring system substituted with a chlorine atom and a carboxylic acid functional group. This compound typically exhibits properties associated with both aromatic and heteroaromatic compounds, such as stability and potential reactivity due to the presence of the carboxylic acid group, which can participate in various chemical reactions, including esterification and amidation. The chlorine substituent can influence the compound's electronic properties, potentially enhancing its reactivity or solubility in organic solvents. Additionally, the presence of the thieno and pyridine moieties may impart biological activity, making it of interest in pharmaceutical research. Its molecular structure allows for various applications in medicinal chemistry, particularly in the development of compounds targeting specific biological pathways. As with many heterocycles, the compound's properties can be further influenced by the presence of other substituents or functional groups, making it a versatile building block in organic synthesis.
Formula:C8H4ClNO2S
InChI:InChI=1S/C8H4ClNO2S/c9-7-4(8(11)12)3-6-5(10-7)1-2-13-6/h1-3H,(H,11,12)
InChI key:InChIKey=JTQYISCVZJCQCW-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1C=C2C(=NC1Cl)C=CS2
Synonyms:
  • Thieno[3,2-b]pyridine-6-carboxylic acid, 5-chloro-
  • 5-Chlorothieno[3,2-b]pyridine-6-carboxylic acid
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