N-(3-Eth­oxy­phen­yl)-4-methyl­benzene­sulfonamide

In the title compound, C(15)H(17)NO(3)S, the two aromatic rings make a dihedral angle of 69.42 (9)° with each other and the bridging C—N—S—C torsion angle is 65.76 (16)°. Weak intra­molecular C—H⋯O inter­actions may affect the mol­ecular conformation. Two neighbouring mol­ecules generate a hydrogen-...

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Detalles Bibliográficos
Autores principales: Aziz-ur-Rehman, Siddiqa, Asia, Akkurt, Mehmet, Abbasi, Muhammad Athar, Jahangir, Muhammad, Khan, Islam Ullah
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006737/
https://www.ncbi.nlm.nih.gov/pubmed/21587907
http://dx.doi.org/10.1107/S1600536810022427
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author Aziz-ur-Rehman,
Siddiqa, Asia
Akkurt, Mehmet
Abbasi, Muhammad Athar
Jahangir, Muhammad
Khan, Islam Ullah
author_facet Aziz-ur-Rehman,
Siddiqa, Asia
Akkurt, Mehmet
Abbasi, Muhammad Athar
Jahangir, Muhammad
Khan, Islam Ullah
author_sort Aziz-ur-Rehman,
collection PubMed
description In the title compound, C(15)H(17)NO(3)S, the two aromatic rings make a dihedral angle of 69.42 (9)° with each other and the bridging C—N—S—C torsion angle is 65.76 (16)°. Weak intra­molecular C—H⋯O inter­actions may affect the mol­ecular conformation. Two neighbouring mol­ecules generate a hydrogen-bonded dimer about a center of inversion through a pair of inter­molecular N—H⋯O inter­actions, forming an R (2) (2)(8) ring motif. Furthermore, two inter­molecular C—H⋯π inter­actions contribute to the stability of the crystal packing.
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spelling pubmed-30067372010-12-30 N-(3-Eth­oxy­phen­yl)-4-methyl­benzene­sulfonamide Aziz-ur-Rehman, Siddiqa, Asia Akkurt, Mehmet Abbasi, Muhammad Athar Jahangir, Muhammad Khan, Islam Ullah Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(17)NO(3)S, the two aromatic rings make a dihedral angle of 69.42 (9)° with each other and the bridging C—N—S—C torsion angle is 65.76 (16)°. Weak intra­molecular C—H⋯O inter­actions may affect the mol­ecular conformation. Two neighbouring mol­ecules generate a hydrogen-bonded dimer about a center of inversion through a pair of inter­molecular N—H⋯O inter­actions, forming an R (2) (2)(8) ring motif. Furthermore, two inter­molecular C—H⋯π inter­actions contribute to the stability of the crystal packing. International Union of Crystallography 2010-06-16 /pmc/articles/PMC3006737/ /pubmed/21587907 http://dx.doi.org/10.1107/S1600536810022427 Text en © Aziz-ur-Rehman 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
Aziz-ur-Rehman,
Siddiqa, Asia
Akkurt, Mehmet
Abbasi, Muhammad Athar
Jahangir, Muhammad
Khan, Islam Ullah
N-(3-Eth­oxy­phen­yl)-4-methyl­benzene­sulfonamide
title N-(3-Eth­oxy­phen­yl)-4-methyl­benzene­sulfonamide
title_full N-(3-Eth­oxy­phen­yl)-4-methyl­benzene­sulfonamide
title_fullStr N-(3-Eth­oxy­phen­yl)-4-methyl­benzene­sulfonamide
title_full_unstemmed N-(3-Eth­oxy­phen­yl)-4-methyl­benzene­sulfonamide
title_short N-(3-Eth­oxy­phen­yl)-4-methyl­benzene­sulfonamide
title_sort n-(3-eth­oxy­phen­yl)-4-methyl­benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006737/
https://www.ncbi.nlm.nih.gov/pubmed/21587907
http://dx.doi.org/10.1107/S1600536810022427
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