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CAS 13130-40-0

:

2-(Acetylamino)-4,5-dimethyl-3-thiophenecarboxylic acid

Description:
2-(Acetylamino)-4,5-dimethyl-3-thiophenecarboxylic acid, with the CAS number 13130-40-0, is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic ring containing sulfur. This compound features an acetylamino group, contributing to its reactivity and potential applications in pharmaceuticals or agrochemicals. The presence of two methyl groups at the 4 and 5 positions of the thiophene ring influences its physical properties, such as solubility and melting point. The carboxylic acid functional group imparts acidic characteristics, allowing for potential interactions in various chemical reactions, including esterification and amidation. This compound may exhibit biological activity, making it of interest in medicinal chemistry. Its synthesis typically involves multi-step organic reactions, and it can be analyzed using techniques such as NMR spectroscopy and mass spectrometry to confirm its structure and purity. Overall, 2-(Acetylamino)-4,5-dimethyl-3-thiophenecarboxylic acid is a versatile compound with significant implications in chemical research and development.
Formula:C9H11NO3S
InChI:InChI=1S/C9H11NO3S/c1-4-5(2)14-8(10-6(3)11)7(4)9(12)13/h1-3H3,(H,10,11)(H,12,13)
InChI key:InChIKey=INDWVNOSVBJHGZ-UHFFFAOYSA-N
SMILES:C(O)(=O)C1=C(NC(C)=O)SC(C)=C1C
Synonyms:
  • 13130-40-0
  • 2-(Acetylamino)-4,5-Dimethylthiophene-3-Carboxylate
  • 2-(Acetylamino)-4,5-dimethyl-3-thiophenecarboxylic acid
  • 2-Acetamido-4,5-dimethylthiophene-3-carboxylic acid
  • 3-Thiophenecarboxylic acid, 2-(acetylamino)-4,5-dimethyl-
  • 3-Thiophenecarboxylic acid, 2-acetamido-4,5-dimethyl-
  • T5Sj Bmv1 Cvq D1 E1 [Wln]
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