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CAS 50901-18-3

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3-(acetylamino)thiophene-2-carboxylic acid

Description:
3-(Acetylamino)thiophene-2-carboxylic acid is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound features an acetylamino group and a carboxylic acid functional group, contributing to its reactivity and potential applications in pharmaceuticals and organic synthesis. The presence of the acetylamino group enhances its solubility in polar solvents, while the carboxylic acid group can participate in hydrogen bonding and acid-base reactions. The thiophene moiety imparts unique electronic properties, making it useful in various chemical reactions, including electrophilic substitutions. Additionally, the compound may exhibit biological activity, which is of interest in medicinal chemistry. Its structural characteristics suggest potential for use in the development of agrochemicals or as intermediates in the synthesis of more complex molecules. Overall, 3-(acetylamino)thiophene-2-carboxylic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C7H7NO3S
InChI:InChI=1/C7H7NO3S/c1-4(9)8-5-2-3-12-6(5)7(10)11/h2-3H,1H3,(H,8,9)(H,10,11)
SMILES:CC(=Nc1ccsc1C(=O)O)O
Synonyms:
  • 3-Acetylaminothiophene-2-carboxylic acid
  • 3-(Acetylamino)-2-Thiophenecarboxylic Acid
  • Buttpark 99\18-20
  • 3-Acetamidothiophene-2-Carboxylic Acid
  • 1H-thieno[3,2-d][1,3]oxazine-2,4-dione
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