N-Cyclo­hexyl-N-ethyl­benzene­sulfonamide

The title compound, C(14)H(21)NO(2)S, synthesized by N-methyl­ation of cyclo­hexyl­amine sulfonamide with ethyl iodide is of inter­est as a precursor to biologically active sulfur-containing heterocyclic compounds. There are two independent mol­ecules in the asymmetric unit. The dihedral angles betw...

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Detalles Bibliográficos
Autores principales: Khan, Islam Ullah, Haider, Zeeshan, Zia-ur-Rehman, Muhammad, Arshad, Muhammad Nadeem, Shafiq, Muhammad
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971250/
https://www.ncbi.nlm.nih.gov/pubmed/21578454
http://dx.doi.org/10.1107/S1600536809044006
Descripción
Sumario:The title compound, C(14)H(21)NO(2)S, synthesized by N-methyl­ation of cyclo­hexyl­amine sulfonamide with ethyl iodide is of inter­est as a precursor to biologically active sulfur-containing heterocyclic compounds. There are two independent mol­ecules in the asymmetric unit. The dihedral angles between the mean planes of the phenyl ring and the cyclo­hexyl ring are 40.29 (11) and 37.91 (13)° in the two mol­ecules.

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