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CAS 350989-81-0

:

methyl 2-amino-4-(4-ethoxyphenyl)thiophene-3-carboxylate

Description:
Methyl 2-amino-4-(4-ethoxyphenyl)thiophene-3-carboxylate, identified by its CAS number 350989-81-0, is a chemical compound characterized by its thiophene core, which is a five-membered aromatic ring containing sulfur. This compound features an amino group and a carboxylate ester, contributing to its potential reactivity and solubility properties. The presence of the ethoxyphenyl substituent enhances its aromatic character and may influence its electronic properties, making it of interest in various applications, including pharmaceuticals and organic synthesis. The methyl ester group can participate in esterification and hydrolysis reactions, while the amino group can engage in hydrogen bonding and nucleophilic reactions. Overall, this compound's unique structure suggests potential utility in medicinal chemistry, particularly in the development of biologically active molecules. Its specific characteristics, such as melting point, solubility, and reactivity, would typically be determined through experimental methods and may vary based on environmental conditions.
Formula:C14H15NO3S
InChI:InChI=1/C14H15NO3S/c1-3-18-10-6-4-9(5-7-10)11-8-19-13(15)12(11)14(16)17-2/h4-8H,3,15H2,1-2H3
SMILES:CCOc1ccc(cc1)c1csc(c1C(=O)OC)N
Synonyms:
  • 2-Amino-4-(4-ethoxy-phenyl)-thiophene-3-carboxylic acid methyl ester
  • 3-Thiophenecarboxylic acid, 2-amino-4-(4-ethoxyphenyl)-, methyl ester
  • Methyl 2-amino-4-(4-ethoxyphenyl)thiophene-3-carboxylate
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