Methyl 2-((((2-chloro-5-nitrophenyl)amino)thioxomethyl)amino)thiophene-3-carboxylate, with CAS number 1024572-87-9, is a synthetic organic compound characterized by its complex structure, which includes a thiophene ring, a carboxylate group, and a nitrophenyl moiety. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, such as potential biological activity and reactivity due to the presence of electron-withdrawing groups like the nitro and chloro substituents. The thioxomethyl and amino groups contribute to its potential as a ligand or in medicinal chemistry applications. Its solubility and stability can vary depending on the solvent and environmental conditions, making it of interest in various chemical and pharmaceutical research contexts. Additionally, the presence of multiple functional groups suggests that it may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, which are valuable in synthetic organic chemistry. Overall, this compound's unique structure and functional groups position it as a candidate for further investigation in drug development and material science.

METHYL 2-((((2-CHLORO-5-NITROPHENYL)AMINO)THIOXOMETHYL)AMINO)THIOPHENE-3-CARBOXYLATE

1024572-87-9: Methyl 2-((((2-chloro-5-nitrophenyl)amino)thioxomethyl)amino)thiophene-3-carboxylate, with CAS number 1024572-87-9, is a synthetic organic compound characterized by its complex structure, which includes a thiophene ring, a carboxylate group, and a nitrophenyl moiety. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, such as potential biological activity and reactivity due to the presence of electron-withdrawing groups like the nitro and chloro substituents. The thioxomethyl and amino groups contribute to its potential as a ligand or in medicinal chemistry applications. Its solubility and stability can vary depending on the solvent and environmental conditions, making it of interest in various chemical and pharmaceutical research contexts. Additionally, the presence of multiple functional groups suggests that it may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, which are valuable in synthetic organic chemistry. Overall, this compound's unique structure and functional groups position it as a candidate for further investigation in drug development and material science.

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CAS 1024572-87-9

METHYL 2-((((2-CHLORO-5-NITROPHENYL)AMINO)THIOXOMETHYL)AMINO)THIOPHENE-3-CARBOXYLATE

methyl 2-((((2-chloro-5-nitrophenyl)amino)thioxomethyl)amino)thiophene-3-carboxylate

Ref: 3D-ZQB57287