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CAS 76360-42-4

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3-Thiophenecarboxylic acid, 2-chloro-, methyl ester

Description:
3-Thiophenecarboxylic acid, 2-chloro-, methyl ester is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic ring containing sulfur. This compound features a carboxylic acid functional group that has been esterified with methanol, resulting in a methyl ester. The presence of a chlorine atom at the second position of the thiophene ring introduces a halogen substituent, which can influence the compound's reactivity and physical properties. Typically, compounds like this exhibit moderate solubility in organic solvents and may have varying degrees of polarity due to the functional groups present. The compound is likely to participate in various chemical reactions, including nucleophilic substitutions and esterification processes. Its applications may extend to pharmaceuticals, agrochemicals, or as intermediates in organic synthesis, owing to the unique properties imparted by the thiophene and chloro substituents. Safety data should be consulted for handling, as halogenated compounds can pose specific health and environmental risks.
Formula:C6H5ClO2S
InChI:InChI=1S/C6H5ClO2S/c1-9-6(8)4-2-3-10-5(4)7/h2-3H,1H3
InChI key:InChIKey=GVIPSISZNQFLRF-UHFFFAOYSA-N
SMILES:C(OC)(=O)C1=C(Cl)SC=C1
Synonyms:
  • 3-Thiophenecarboxylic acid, 2-chloro-, methyl ester
  • Methyl 2-chlorothiophene-3-carboxylate
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