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CAS 350989-69-4

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Methyl 2-amino-4-(4-ethylphenyl)-5-methyl-3-thiophenecarboxylate

Description:
Methyl 2-amino-4-(4-ethylphenyl)-5-methyl-3-thiophenecarboxylate, identified by its CAS number 350989-69-4, is an organic compound characterized by its complex structure, which includes a thiophene ring and various functional groups. This compound features an amino group, which contributes to its potential as a building block in pharmaceuticals and agrochemicals. The presence of the ethylphenyl substituent enhances its hydrophobic characteristics, potentially influencing its solubility and biological activity. The methyl ester group indicates that it can undergo hydrolysis to yield the corresponding carboxylic acid, which may exhibit different reactivity and properties. Additionally, the thiophene moiety is known for its electronic properties, making this compound of interest in materials science and organic electronics. Overall, the unique combination of functional groups and structural features suggests that this compound may exhibit interesting chemical reactivity and biological activity, warranting further investigation in various applications.
Formula:C15H17NO2S
InChI:InChI=1S/C15H17NO2S/c1-4-10-5-7-11(8-6-10)12-9(2)19-14(16)13(12)15(17)18-3/h5-8H,4,16H2,1-3H3
InChI key:InChIKey=LPKMNMLKXYDWMD-UHFFFAOYSA-N
SMILES:C(OC)(=O)C=1C(=C(C)SC1N)C2=CC=C(CC)C=C2
Synonyms:
  • 3-Thiophenecarboxylic acid, 2-amino-4-(4-ethylphenyl)-5-methyl-, methyl ester
  • Methyl 2-amino-4-(4-ethylphenyl)-5-methyl-3-thiophenecarboxylate
  • Methyl 2-amino-4-(4-ethylphenyl)-5-methylthiophene-3-carboxylate
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