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
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author Khan, Islam Ullah
Haider, Zeeshan
Zia-ur-Rehman, Muhammad
Arshad, Muhammad Nadeem
Shafiq, Muhammad
author_facet Khan, Islam Ullah
Haider, Zeeshan
Zia-ur-Rehman, Muhammad
Arshad, Muhammad Nadeem
Shafiq, Muhammad
author_sort Khan, Islam Ullah
collection PubMed
description 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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spelling pubmed-29712502010-12-30 N-Cyclo­hexyl-N-ethyl­benzene­sulfonamide Khan, Islam Ullah Haider, Zeeshan Zia-ur-Rehman, Muhammad Arshad, Muhammad Nadeem Shafiq, Muhammad Acta Crystallogr Sect E Struct Rep Online Organic Papers 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. International Union of Crystallography 2009-10-28 /pmc/articles/PMC2971250/ /pubmed/21578454 http://dx.doi.org/10.1107/S1600536809044006 Text en © Khan et al. 2009 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Khan, Islam Ullah
Haider, Zeeshan
Zia-ur-Rehman, Muhammad
Arshad, Muhammad Nadeem
Shafiq, Muhammad
N-Cyclo­hexyl-N-ethyl­benzene­sulfonamide
title N-Cyclo­hexyl-N-ethyl­benzene­sulfonamide
title_full N-Cyclo­hexyl-N-ethyl­benzene­sulfonamide
title_fullStr N-Cyclo­hexyl-N-ethyl­benzene­sulfonamide
title_full_unstemmed N-Cyclo­hexyl-N-ethyl­benzene­sulfonamide
title_short N-Cyclo­hexyl-N-ethyl­benzene­sulfonamide
title_sort n-cyclo­hexyl-n-ethyl­benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971250/
https://www.ncbi.nlm.nih.gov/pubmed/21578454
http://dx.doi.org/10.1107/S1600536809044006
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AT ziaurrehmanmuhammad ncyclohexylnethylbenzenesulfonamide
AT arshadmuhammadnadeem ncyclohexylnethylbenzenesulfonamide
AT shafiqmuhammad ncyclohexylnethylbenzenesulfonamide

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