N-Cyclo­hexyl-N-(prop-2-en-1-yl)benzene­sulfonamide

The title compound, C(15)H(21)NO(2)S, synthesized by N-alkyl­ation of cyclo­hexyl­amine benzene­sulfonamide with allyl iodide, is of inter­est as a precursor to biologically active sulfur-containing heterocyclic compounds. The cyclo­hexane ring is in a chair form and its mean plane makes a dihedral...

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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/PMC2972124/
https://www.ncbi.nlm.nih.gov/pubmed/21578829
http://dx.doi.org/10.1107/S1600536809048077
Descripción
Sumario:The title compound, C(15)H(21)NO(2)S, synthesized by N-alkyl­ation of cyclo­hexyl­amine benzene­sulfonamide with allyl iodide, is of inter­est as a precursor to biologically active sulfur-containing heterocyclic compounds. The cyclo­hexane ring is in a chair form and its mean plane makes a dihedral angle of 53.84 (12)° with the phenyl ring.

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