N-[4-(p-Toluenesulfonamido)phen­ylsulfon­yl]acetamide

In the title compound, C(15)H(16)N(2)O(5)S(2), the dihedral between the two aromatic rings is 81.33 (6)°. In the crystal, pairs of N—H⋯O hydrogen bonds link the mol­ecules into centrosymmetric dimers, which are further connected via N—H⋯O hydrogen bonds into a chain running along [[Image: see text]0...

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Detalles Bibliográficos
Autores principales: Ashfaq, Muhammad, Khan, Islam Ullah, Arshad, Muhammad Nadeem, Ahmad, Hamad, Asghar, Muhammad Nadeem
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979981/
https://www.ncbi.nlm.nih.gov/pubmed/21579732
http://dx.doi.org/10.1107/S1600536809055706
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author Ashfaq, Muhammad
Khan, Islam Ullah
Arshad, Muhammad Nadeem
Ahmad, Hamad
Asghar, Muhammad Nadeem
author_facet Ashfaq, Muhammad
Khan, Islam Ullah
Arshad, Muhammad Nadeem
Ahmad, Hamad
Asghar, Muhammad Nadeem
author_sort Ashfaq, Muhammad
collection PubMed
description In the title compound, C(15)H(16)N(2)O(5)S(2), the dihedral between the two aromatic rings is 81.33 (6)°. In the crystal, pairs of N—H⋯O hydrogen bonds link the mol­ecules into centrosymmetric dimers, which are further connected via N—H⋯O hydrogen bonds into a chain running along [[Image: see text]01].
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spelling pubmed-29799812010-12-30 N-[4-(p-Toluenesulfonamido)phen­ylsulfon­yl]acetamide Ashfaq, Muhammad Khan, Islam Ullah Arshad, Muhammad Nadeem Ahmad, Hamad Asghar, Muhammad Nadeem Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(16)N(2)O(5)S(2), the dihedral between the two aromatic rings is 81.33 (6)°. In the crystal, pairs of N—H⋯O hydrogen bonds link the mol­ecules into centrosymmetric dimers, which are further connected via N—H⋯O hydrogen bonds into a chain running along [[Image: see text]01]. International Union of Crystallography 2010-01-09 /pmc/articles/PMC2979981/ /pubmed/21579732 http://dx.doi.org/10.1107/S1600536809055706 Text en © Ashfaq 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
Ashfaq, Muhammad
Khan, Islam Ullah
Arshad, Muhammad Nadeem
Ahmad, Hamad
Asghar, Muhammad Nadeem
N-[4-(p-Toluenesulfonamido)phen­ylsulfon­yl]acetamide
title N-[4-(p-Toluenesulfonamido)phen­ylsulfon­yl]acetamide
title_full N-[4-(p-Toluenesulfonamido)phen­ylsulfon­yl]acetamide
title_fullStr N-[4-(p-Toluenesulfonamido)phen­ylsulfon­yl]acetamide
title_full_unstemmed N-[4-(p-Toluenesulfonamido)phen­ylsulfon­yl]acetamide
title_short N-[4-(p-Toluenesulfonamido)phen­ylsulfon­yl]acetamide
title_sort n-[4-(p-toluenesulfonamido)phen­ylsulfon­yl]acetamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979981/
https://www.ncbi.nlm.nih.gov/pubmed/21579732
http://dx.doi.org/10.1107/S1600536809055706
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