1-((4-(tert-butyl)phenyl)sulfonyl)-4-(3-chloro-5-(trifluoromethyl)(2-pyridyl))-1,4-diazaperhydroepine is a complex organic compound characterized by its unique structural features, including a diazaperhydroepine core, which contributes to its potential biological activity. The presence of a tert-butyl group enhances its lipophilicity, while the sulfonyl group may impart specific reactivity and solubility characteristics. The incorporation of a chlorinated pyridine moiety, particularly with a trifluoromethyl substituent, suggests potential applications in medicinal chemistry, possibly as a pharmaceutical agent. This compound may exhibit interesting interactions with biological targets due to its diverse functional groups, which can influence its pharmacokinetic properties. Additionally, the presence of halogens and sulfonyl groups often enhances the compound's stability and reactivity, making it a candidate for further investigation in drug development or as a chemical probe in biological studies. Overall, this compound's intricate structure and functional diversity position it as a noteworthy subject for research in organic and medicinal chemistry.

1-((4-(TERT-BUTYL)PHENYL)SULFONYL)-4-(3-CHLORO-5-(TRIFLUOROMETHYL)(2-PYRIDYL))-1,4-DIAZAPERHYDROEPINE

1022234-53-2: 1-((4-(tert-butyl)phenyl)sulfonyl)-4-(3-chloro-5-(trifluoromethyl)(2-pyridyl))-1,4-diazaperhydroepine is a complex organic compound characterized by its unique structural features, including a diazaperhydroepine core, which contributes to its potential biological activity. The presence of a tert-butyl group enhances its lipophilicity, while the sulfonyl group may impart specific reactivity and solubility characteristics. The incorporation of a chlorinated pyridine moiety, particularly with a trifluoromethyl substituent, suggests potential applications in medicinal chemistry, possibly as a pharmaceutical agent. This compound may exhibit interesting interactions with biological targets due to its diverse functional groups, which can influence its pharmacokinetic properties. Additionally, the presence of halogens and sulfonyl groups often enhances the compound's stability and reactivity, making it a candidate for further investigation in drug development or as a chemical probe in biological studies. Overall, this compound's intricate structure and functional diversity position it as a noteworthy subject for research in organic and medicinal chemistry.

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CAS 1022234-53-2

1-((4-(TERT-BUTYL)PHENYL)SULFONYL)-4-(3-CHLORO-5-(TRIFLUOROMETHYL)(2-PYRIDYL))-1,4-DIAZAPERHYDROEPINE

1-((4-(tert-butyl)phenyl)sulfonyl)-4-(3-chloro-5-(trifluoromethyl)(2-pyridyl))-1,4-diazaperhydroepine

Ref: 3D-XQB23453