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CAS 4815-25-2

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Methyl 2-amino-4-ethyl-5-methyl-3-thiophenecarboxylate

Description:
Methyl 2-amino-4-ethyl-5-methyl-3-thiophenecarboxylate, with the CAS number 4815-25-2, is an organic compound characterized by its thiophene ring structure, which contributes to its unique chemical properties. This compound features an amino group, an ethyl group, and a methyl group, indicating it has multiple functional groups that can participate in various chemical reactions. The presence of the carboxylate ester functional group suggests it can undergo hydrolysis, transesterification, and other reactions typical of esters. Its thiophene moiety may impart aromatic characteristics, influencing its reactivity and stability. The compound is likely to be soluble in organic solvents due to its non-polar thiophene ring, while the polar amino and carboxylate groups may enhance solubility in polar solvents. Methyl 2-amino-4-ethyl-5-methyl-3-thiophenecarboxylate may have applications in pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis, although specific applications would depend on further research into its biological activity and reactivity.
Formula:C9H13NO2S
InChI:InChI=1S/C9H13NO2S/c1-4-6-5(2)13-8(10)7(6)9(11)12-3/h4,10H2,1-3H3
InChI key:InChIKey=ODDNCALHGKYZJB-UHFFFAOYSA-N
SMILES:C(OC)(=O)C=1C(CC)=C(C)SC1N
Synonyms:
  • 2-Amino-4-Ethyl-5-Methylthiophene-3-Carboxylic Acid Methyl Ester
  • 2-Amino-4-ethyl-5-methyl-thiophene-3-carboxylic acid methyl ester
  • 3-Thiophenecarboxylic acid, 2-amino-4-ethyl-5-methyl-, methyl ester
  • Methyl 2-amino-4-ethyl-5-methyl-3-thiophenecarboxylate
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