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N-(3-Meth­oxy­benzo­yl)-4-methyl­benzene­sulfonamide

In the title compound, C(15)H(15)NO(4)S, the dihedral angle between the benzene rings is 88.87 (1)°. In the crystal, adjacent mol­ecules form inversion dimers through pairs of strong N—H⋯O hydrogen bonds, generating R (2) (2)(8) loops. Two C—H⋯π inter­actions and an aromatic π–π inter­action [centro...

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Autores principales: Sreenivasa, S., Palakshamurthy, B. S., Lohith, T. N., Mohan, N. R., Kumar, Vijith, Suchetan, P. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793760/
https://www.ncbi.nlm.nih.gov/pubmed/24109347
http://dx.doi.org/10.1107/S1600536813019107
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author Sreenivasa, S.
Palakshamurthy, B. S.
Lohith, T. N.
Mohan, N. R.
Kumar, Vijith
Suchetan, P. A.
author_facet Sreenivasa, S.
Palakshamurthy, B. S.
Lohith, T. N.
Mohan, N. R.
Kumar, Vijith
Suchetan, P. A.
author_sort Sreenivasa, S.
collection PubMed
description In the title compound, C(15)H(15)NO(4)S, the dihedral angle between the benzene rings is 88.87 (1)°. In the crystal, adjacent mol­ecules form inversion dimers through pairs of strong N—H⋯O hydrogen bonds, generating R (2) (2)(8) loops. Two C—H⋯π inter­actions and an aromatic π–π inter­action [centroid–centroid separation = 3.8191 (1) Å] are also observed.
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spelling pubmed-37937602013-10-09 N-(3-Meth­oxy­benzo­yl)-4-methyl­benzene­sulfonamide Sreenivasa, S. Palakshamurthy, B. S. Lohith, T. N. Mohan, N. R. Kumar, Vijith Suchetan, P. A. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(15)NO(4)S, the dihedral angle between the benzene rings is 88.87 (1)°. In the crystal, adjacent mol­ecules form inversion dimers through pairs of strong N—H⋯O hydrogen bonds, generating R (2) (2)(8) loops. Two C—H⋯π inter­actions and an aromatic π–π inter­action [centroid–centroid separation = 3.8191 (1) Å] are also observed. International Union of Crystallography 2013-07-17 /pmc/articles/PMC3793760/ /pubmed/24109347 http://dx.doi.org/10.1107/S1600536813019107 Text en © Sreenivasa et al. 2013 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
Sreenivasa, S.
Palakshamurthy, B. S.
Lohith, T. N.
Mohan, N. R.
Kumar, Vijith
Suchetan, P. A.
N-(3-Meth­oxy­benzo­yl)-4-methyl­benzene­sulfonamide
title N-(3-Meth­oxy­benzo­yl)-4-methyl­benzene­sulfonamide
title_full N-(3-Meth­oxy­benzo­yl)-4-methyl­benzene­sulfonamide
title_fullStr N-(3-Meth­oxy­benzo­yl)-4-methyl­benzene­sulfonamide
title_full_unstemmed N-(3-Meth­oxy­benzo­yl)-4-methyl­benzene­sulfonamide
title_short N-(3-Meth­oxy­benzo­yl)-4-methyl­benzene­sulfonamide
title_sort n-(3-meth­oxy­benzo­yl)-4-methyl­benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793760/
https://www.ncbi.nlm.nih.gov/pubmed/24109347
http://dx.doi.org/10.1107/S1600536813019107
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