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CAS 37572-23-9

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3-Amino-5-(4-methoxyphenyl)thiophene-2-carboxylic acid methyl ester

Description:
3-Amino-5-(4-methoxyphenyl)thiophene-2-carboxylic acid methyl ester is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features an amino group (-NH2) and a methoxyphenyl group, contributing to its potential as a building block in pharmaceuticals and organic synthesis. The presence of the carboxylic acid methyl ester functional group indicates that it can undergo hydrolysis to yield the corresponding carboxylic acid, which may enhance its reactivity and solubility in various solvents. The methoxy group enhances the compound's electron-donating properties, potentially influencing its reactivity and interactions with biological targets. This compound may exhibit interesting biological activities, making it a candidate for further research in medicinal chemistry. Its molecular structure suggests potential applications in drug development, particularly in the design of compounds with specific pharmacological properties. As with many organic compounds, its stability, solubility, and reactivity can vary based on environmental conditions and the presence of other functional groups.
Formula:C13H13NO3S
InChI:InChI=1/C13H13NO3S/c1-16-9-5-3-8(4-6-9)11-7-10(14)12(18-11)13(15)17-2/h3-7H,14H2,1-2H3
SMILES:COc1ccc(cc1)c1cc(c(C(=O)OC)s1)N
Synonyms:
  • 2-Thiophenecarboxylic acid, 3-amino-5-(4-methoxyphenyl)-, methyl ester
  • Methyl 3-Amino-5-(4-Methoxyphenyl)Thiophene-2-Carboxylate
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