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CAS 350990-26-0

:

methyl 2-amino-4-(2,5-dimethylphenyl)thiophene-3-carboxylate

Description:
Methyl 2-amino-4-(2,5-dimethylphenyl)thiophene-3-carboxylate, with the CAS number 350990-26-0, 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 and a carboxylate ester, contributing to its potential reactivity and solubility properties. The presence of the 2,5-dimethylphenyl substituent enhances its hydrophobic characteristics and may influence its biological activity. Typically, compounds of this nature can exhibit a range of properties, including potential pharmacological effects, due to the presence of functional groups that can participate in hydrogen bonding and other intermolecular interactions. The methyl ester group may also affect the compound's stability and reactivity, making it a candidate for further chemical modifications. Overall, this compound's unique structure suggests potential applications in medicinal chemistry and materials science, although specific biological activities and applications would require further investigation.
Formula:C14H15NO2S
InChI:InChI=1/C14H15NO2S/c1-8-4-5-9(2)10(6-8)11-7-18-13(15)12(11)14(16)17-3/h4-7H,15H2,1-3H3
SMILES:Cc1ccc(C)c(c1)c1csc(c1C(=O)OC)N
Synonyms:
  • 3-Thiophenecarboxylic acid, 2-amino-4-(2,5-dimethylphenyl)-, methyl ester
  • Methyl 2-amino-4-(2,5-dimethylphenyl)thiophene-3-carboxylate
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