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N-(2-Hydroxyphenyl)-4-methylbenzenesulfonamide
In the title compound, C(13)H(13)NO(3)S, the dihedral angle between the benzene rings is 64.15 (7)° and the C—S—N—C torsion angle is −57.18 (12)°. An intramolecular N—H⋯O hydrogen bond closes an S(5) ring. In the crystal, O—H⋯O hydrogen bonds link the molecules into C(8) chains propagating in [100...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914092/ https://www.ncbi.nlm.nih.gov/pubmed/24526996 http://dx.doi.org/10.1107/S1600536813033394 |
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author | Mohamed, Shaaban K. Akkurt, Mehmet Kariuki, Benson M. Ali, Ali M. Albayati, Mustafa R. |
author_facet | Mohamed, Shaaban K. Akkurt, Mehmet Kariuki, Benson M. Ali, Ali M. Albayati, Mustafa R. |
author_sort | Mohamed, Shaaban K. |
collection | PubMed |
description | In the title compound, C(13)H(13)NO(3)S, the dihedral angle between the benzene rings is 64.15 (7)° and the C—S—N—C torsion angle is −57.18 (12)°. An intramolecular N—H⋯O hydrogen bond closes an S(5) ring. In the crystal, O—H⋯O hydrogen bonds link the molecules into C(8) chains propagating in [100]. Weak C—H⋯π interactions are also observed. |
format | Online Article Text |
id | pubmed-3914092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-39140922014-02-13 N-(2-Hydroxyphenyl)-4-methylbenzenesulfonamide Mohamed, Shaaban K. Akkurt, Mehmet Kariuki, Benson M. Ali, Ali M. Albayati, Mustafa R. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(13)NO(3)S, the dihedral angle between the benzene rings is 64.15 (7)° and the C—S—N—C torsion angle is −57.18 (12)°. An intramolecular N—H⋯O hydrogen bond closes an S(5) ring. In the crystal, O—H⋯O hydrogen bonds link the molecules into C(8) chains propagating in [100]. Weak C—H⋯π interactions are also observed. International Union of Crystallography 2013-12-14 /pmc/articles/PMC3914092/ /pubmed/24526996 http://dx.doi.org/10.1107/S1600536813033394 Text en © Mohamed et al. 2014 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 Mohamed, Shaaban K. Akkurt, Mehmet Kariuki, Benson M. Ali, Ali M. Albayati, Mustafa R. N-(2-Hydroxyphenyl)-4-methylbenzenesulfonamide |
title |
N-(2-Hydroxyphenyl)-4-methylbenzenesulfonamide |
title_full |
N-(2-Hydroxyphenyl)-4-methylbenzenesulfonamide |
title_fullStr |
N-(2-Hydroxyphenyl)-4-methylbenzenesulfonamide |
title_full_unstemmed |
N-(2-Hydroxyphenyl)-4-methylbenzenesulfonamide |
title_short |
N-(2-Hydroxyphenyl)-4-methylbenzenesulfonamide |
title_sort | n-(2-hydroxyphenyl)-4-methylbenzenesulfonamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914092/ https://www.ncbi.nlm.nih.gov/pubmed/24526996 http://dx.doi.org/10.1107/S1600536813033394 |
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