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CAS 15854-10-1

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Ethyl 2-amino-4-(2,4-dimethylphenyl)-3-thiophenecarboxylate

Description:
Ethyl 2-amino-4-(2,4-dimethylphenyl)-3-thiophenecarboxylate, with the CAS number 15854-10-1, is an organic compound characterized by its complex structure, which includes an ethyl ester group, an amino group, and a thiophene ring. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, such as moderate solubility in organic solvents and potential reactivity due to the presence of the amino group. The thiophene moiety contributes to its aromatic character, while the dimethylphenyl substituent can influence its electronic properties and steric hindrance. Ethyl 2-amino-4-(2,4-dimethylphenyl)-3-thiophenecarboxylate may be of interest in various fields, including medicinal chemistry and materials science, due to its potential biological activity and utility in synthesizing other chemical entities. Its specific reactivity and interactions would depend on the functional groups present, making it a candidate for further research in drug development or as a building block in organic synthesis.
Formula:C15H17NO2S
InChI:InChI=1S/C15H17NO2S/c1-4-18-15(17)13-12(8-19-14(13)16)11-6-5-9(2)7-10(11)3/h5-8H,4,16H2,1-3H3
InChI key:InChIKey=XBGBEIKHJJZZLM-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C=1C(=CSC1N)C2=C(C)C=C(C)C=C2
Synonyms:
  • 3-Thiophenecarboxylic Acid, 2-Amino-4-(2,4-Dimethylphenyl)-, Ethyl Ester
  • 3-Thiophenecarboxylic acid, 2-amino-4-(2,4-xylyl)-, ethyl ester
  • Ethyl 2-Amino-4-(2,4-Dimethylphenyl)Thiophene-3-Carboxylate
  • Ethyl 2-amino-4-(2,4-dimethylphenyl)-3-thiophenecarboxylate
  • 2-Amino-4-(2,4-dimethyl-phenyl)-thiophene-3-carboxylic acid ethyl ester
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