N-[4-(N-Cyclo­hexyl­sulfamo­yl)phen­yl]acetamide

In the title compound, C(14)H(20)N(2)O(3)S, the cyclo­hexyl ring adopts a chair conformation: the four coplanar C atoms of this ring make a dihedral angle of 64.8 (2)° with the benzene ring. In the mol­ecule, an intra­molecular C—H⋯O contact generates an S(6) ring motif. In the crystal structure, mo...

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Detalles Bibliográficos
Autores principales: Khan, Islam Ullah, Akkurt, Mehmet, Anwar, Faiza, Sharif, Shahzad
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983925/
https://www.ncbi.nlm.nih.gov/pubmed/21580690
http://dx.doi.org/10.1107/S160053681000961X
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author Khan, Islam Ullah
Akkurt, Mehmet
Anwar, Faiza
Sharif, Shahzad
author_facet Khan, Islam Ullah
Akkurt, Mehmet
Anwar, Faiza
Sharif, Shahzad
author_sort Khan, Islam Ullah
collection PubMed
description In the title compound, C(14)H(20)N(2)O(3)S, the cyclo­hexyl ring adopts a chair conformation: the four coplanar C atoms of this ring make a dihedral angle of 64.8 (2)° with the benzene ring. In the mol­ecule, an intra­molecular C—H⋯O contact generates an S(6) ring motif. In the crystal structure, mol­ecules are linked via inter­molecular N—H⋯O hydrogen bonds into two-dimensional layers propagating in (100).
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spelling pubmed-29839252010-12-30 N-[4-(N-Cyclo­hexyl­sulfamo­yl)phen­yl]acetamide Khan, Islam Ullah Akkurt, Mehmet Anwar, Faiza Sharif, Shahzad Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(14)H(20)N(2)O(3)S, the cyclo­hexyl ring adopts a chair conformation: the four coplanar C atoms of this ring make a dihedral angle of 64.8 (2)° with the benzene ring. In the mol­ecule, an intra­molecular C—H⋯O contact generates an S(6) ring motif. In the crystal structure, mol­ecules are linked via inter­molecular N—H⋯O hydrogen bonds into two-dimensional layers propagating in (100). International Union of Crystallography 2010-03-20 /pmc/articles/PMC2983925/ /pubmed/21580690 http://dx.doi.org/10.1107/S160053681000961X Text en © Khan et al. 2010 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
Akkurt, Mehmet
Anwar, Faiza
Sharif, Shahzad
N-[4-(N-Cyclo­hexyl­sulfamo­yl)phen­yl]acetamide
title N-[4-(N-Cyclo­hexyl­sulfamo­yl)phen­yl]acetamide
title_full N-[4-(N-Cyclo­hexyl­sulfamo­yl)phen­yl]acetamide
title_fullStr N-[4-(N-Cyclo­hexyl­sulfamo­yl)phen­yl]acetamide
title_full_unstemmed N-[4-(N-Cyclo­hexyl­sulfamo­yl)phen­yl]acetamide
title_short N-[4-(N-Cyclo­hexyl­sulfamo­yl)phen­yl]acetamide
title_sort n-[4-(n-cyclo­hexyl­sulfamo­yl)phen­yl]acetamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983925/
https://www.ncbi.nlm.nih.gov/pubmed/21580690
http://dx.doi.org/10.1107/S160053681000961X
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AT akkurtmehmet n4ncyclohexylsulfamoylphenylacetamide
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AT sharifshahzad n4ncyclohexylsulfamoylphenylacetamide

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