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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...
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/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. |
format | Online Article Text |
id | pubmed-3793760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
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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