4-Chloro-N-cyclo­hexyl­benzene­sulfonamide

The title compound, C(12)H(16)ClNO(2)S, adopts an L-shaped conformation, with the central C—S—N—C torsion angle being −78.0 (2)°. The cyclo­hexyl ring adopts a chair conformation. In the crystal, adjacent mol­ecules are connected by pairs of N—H⋯O hydrogen bonds around an inversion centre, forming c...

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Autores principales: Sharif, Shahzad, Mughal, Shumaila Younas, Khan, Islam Ullah, Akkurt, Mehmet, Khan, Muneeb Hayat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275220/
https://www.ncbi.nlm.nih.gov/pubmed/22347076
http://dx.doi.org/10.1107/S1600536812001870
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author Sharif, Shahzad
Mughal, Shumaila Younas
Khan, Islam Ullah
Akkurt, Mehmet
Khan, Muneeb Hayat
author_facet Sharif, Shahzad
Mughal, Shumaila Younas
Khan, Islam Ullah
Akkurt, Mehmet
Khan, Muneeb Hayat
author_sort Sharif, Shahzad
collection PubMed
description The title compound, C(12)H(16)ClNO(2)S, adopts an L-shaped conformation, with the central C—S—N—C torsion angle being −78.0 (2)°. The cyclo­hexyl ring adopts a chair conformation. In the crystal, adjacent mol­ecules are connected by pairs of N—H⋯O hydrogen bonds around an inversion centre, forming cyclic dimers [graph set R (2) (2)(8)].
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spelling pubmed-32752202012-02-15 4-Chloro-N-cyclo­hexyl­benzene­sulfonamide Sharif, Shahzad Mughal, Shumaila Younas Khan, Islam Ullah Akkurt, Mehmet Khan, Muneeb Hayat Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(12)H(16)ClNO(2)S, adopts an L-shaped conformation, with the central C—S—N—C torsion angle being −78.0 (2)°. The cyclo­hexyl ring adopts a chair conformation. In the crystal, adjacent mol­ecules are connected by pairs of N—H⋯O hydrogen bonds around an inversion centre, forming cyclic dimers [graph set R (2) (2)(8)]. International Union of Crystallography 2012-01-21 /pmc/articles/PMC3275220/ /pubmed/22347076 http://dx.doi.org/10.1107/S1600536812001870 Text en © Sharif et al. 2012 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
Sharif, Shahzad
Mughal, Shumaila Younas
Khan, Islam Ullah
Akkurt, Mehmet
Khan, Muneeb Hayat
4-Chloro-N-cyclo­hexyl­benzene­sulfonamide
title 4-Chloro-N-cyclo­hexyl­benzene­sulfonamide
title_full 4-Chloro-N-cyclo­hexyl­benzene­sulfonamide
title_fullStr 4-Chloro-N-cyclo­hexyl­benzene­sulfonamide
title_full_unstemmed 4-Chloro-N-cyclo­hexyl­benzene­sulfonamide
title_short 4-Chloro-N-cyclo­hexyl­benzene­sulfonamide
title_sort 4-chloro-n-cyclo­hexyl­benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275220/
https://www.ncbi.nlm.nih.gov/pubmed/22347076
http://dx.doi.org/10.1107/S1600536812001870
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AT akkurtmehmet 4chloroncyclohexylbenzenesulfonamide
AT khanmuneebhayat 4chloroncyclohexylbenzenesulfonamide

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