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CAS 350990-31-7

:

ethyl 2-amino-4-(2,5-dimethylphenyl)-5-methylthiophene-3-carboxylate

Description:
Ethyl 2-amino-4-(2,5-dimethylphenyl)-5-methylthiophene-3-carboxylate is a chemical compound characterized by its complex structure, which includes a thiophene ring, an amino group, and an ester functional group. This compound features a substituted thiophene, which contributes to its potential biological activity and chemical reactivity. The presence of the ethyl ester group enhances its solubility in organic solvents, making it suitable for various applications in organic synthesis and medicinal chemistry. The 2,5-dimethylphenyl substituent adds steric bulk and may influence the compound's interactions with biological targets. Additionally, the amino group can participate in hydrogen bonding, which may affect its pharmacokinetic properties. Overall, this compound's unique structural features suggest potential utility in drug development or as a building block in organic synthesis, although specific biological activities and applications would require further investigation.
Formula:C16H19NO2S
InChI:InChI=1/C16H19NO2S/c1-5-19-16(18)14-13(11(4)20-15(14)17)12-8-9(2)6-7-10(12)3/h6-8H,5,17H2,1-4H3
SMILES:CCOC(=O)c1c(c(C)sc1N)c1cc(C)ccc1C
Synonyms:
  • 3-Thiophenecarboxylic acid, 2-amino-4-(2,5-dimethylphenyl)-5-methyl-, ethyl ester
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