The chemical substance known as 4-((3-bromophenyl)sulfonyl)-N-(1-(thiophen-2-yl)ethyl)piperazine-1-carboxamide is a complex organic compound characterized by its piperazine core, which is a six-membered ring containing two nitrogen atoms. This compound features a sulfonamide functional group, indicated by the presence of a sulfonyl moiety attached to a bromophenyl group, which contributes to its potential biological activity. The thiophene ring, a five-membered aromatic heterocycle containing sulfur, is also a notable feature, enhancing the compound's electronic properties and possibly its interaction with biological targets. The presence of the carboxamide group suggests potential for hydrogen bonding, which may influence solubility and reactivity. Overall, this compound may exhibit interesting pharmacological properties, making it a candidate for further research in medicinal chemistry. Its specific characteristics, such as solubility, stability, and reactivity, would depend on the molecular interactions and the environment in which it is studied.

4-((3-bromophenyl)sulfonyl)-N-(1-(thiophen-2-yl)ethyl)piperazine-1-carboxamide

1090528-71-4: The chemical substance known as 4-((3-bromophenyl)sulfonyl)-N-(1-(thiophen-2-yl)ethyl)piperazine-1-carboxamide is a complex organic compound characterized by its piperazine core, which is a six-membered ring containing two nitrogen atoms. This compound features a sulfonamide functional group, indicated by the presence of a sulfonyl moiety attached to a bromophenyl group, which contributes to its potential biological activity. The thiophene ring, a five-membered aromatic heterocycle containing sulfur, is also a notable feature, enhancing the compound's electronic properties and possibly its interaction with biological targets. The presence of the carboxamide group suggests potential for hydrogen bonding, which may influence solubility and reactivity. Overall, this compound may exhibit interesting pharmacological properties, making it a candidate for further research in medicinal chemistry. Its specific characteristics, such as solubility, stability, and reactivity, would depend on the molecular interactions and the environment in which it is studied.

<p>Applications T6167923 is a novel inhibitor of MyD88-dependent signaling pathways, disrupting MyD88 homodimeric formation, which is critical for its signaling function<br>References Olson, Mark A., et al.:Sci. Rep.,5, 14246 (2015);<br></p>

CAS 1090528-71-4

4-((3-bromophenyl)sulfonyl)-N-(1-(thiophen-2-yl)ethyl)piperazine-1-carboxamide

T6167923

Ref: TR-T966338