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N-Methyl-N-nitroso-p-toluenesulfonamide
The crystal structure of the title compound, C(8)H(10)N(2)O(3)S, displays predominant C—H⋯O hydrogen-bonding and π–π stacking interactions. The hydrogen bonds are between the O atoms of the sulfonyl group and H atoms on methyl groups. The π–π stacking interactions occur between adjacent aromatic r...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4120625/ https://www.ncbi.nlm.nih.gov/pubmed/25161568 http://dx.doi.org/10.1107/S1600536814013518 |
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author | Rai, Kartik Wu, Vincent Gupta, Priya Laviska, David A. Chan, Benny C. |
author_facet | Rai, Kartik Wu, Vincent Gupta, Priya Laviska, David A. Chan, Benny C. |
author_sort | Rai, Kartik |
collection | PubMed |
description | The crystal structure of the title compound, C(8)H(10)N(2)O(3)S, displays predominant C—H⋯O hydrogen-bonding and π–π stacking interactions. The hydrogen bonds are between the O atoms of the sulfonyl group and H atoms on methyl groups. The π–π stacking interactions occur between adjacent aromatic rings, with a centroid–centroid distance of 3.868 (11) Å. These interactions lead to the formation of chains parallel to (101). |
format | Online Article Text |
id | pubmed-4120625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-41206252014-08-26 N-Methyl-N-nitroso-p-toluenesulfonamide Rai, Kartik Wu, Vincent Gupta, Priya Laviska, David A. Chan, Benny C. Acta Crystallogr Sect E Struct Rep Online Organic Papers The crystal structure of the title compound, C(8)H(10)N(2)O(3)S, displays predominant C—H⋯O hydrogen-bonding and π–π stacking interactions. The hydrogen bonds are between the O atoms of the sulfonyl group and H atoms on methyl groups. The π–π stacking interactions occur between adjacent aromatic rings, with a centroid–centroid distance of 3.868 (11) Å. These interactions lead to the formation of chains parallel to (101). International Union of Crystallography 2014-06-14 /pmc/articles/PMC4120625/ /pubmed/25161568 http://dx.doi.org/10.1107/S1600536814013518 Text en © Rai 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 Rai, Kartik Wu, Vincent Gupta, Priya Laviska, David A. Chan, Benny C. N-Methyl-N-nitroso-p-toluenesulfonamide |
title |
N-Methyl-N-nitroso-p-toluenesulfonamide |
title_full |
N-Methyl-N-nitroso-p-toluenesulfonamide |
title_fullStr |
N-Methyl-N-nitroso-p-toluenesulfonamide |
title_full_unstemmed |
N-Methyl-N-nitroso-p-toluenesulfonamide |
title_short |
N-Methyl-N-nitroso-p-toluenesulfonamide |
title_sort | n-methyl-n-nitroso-p-toluenesulfonamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4120625/ https://www.ncbi.nlm.nih.gov/pubmed/25161568 http://dx.doi.org/10.1107/S1600536814013518 |
work_keys_str_mv | AT raikartik nmethylnnitrosoptoluenesulfonamide AT wuvincent nmethylnnitrosoptoluenesulfonamide AT guptapriya nmethylnnitrosoptoluenesulfonamide AT laviskadavida nmethylnnitrosoptoluenesulfonamide AT chanbennyc nmethylnnitrosoptoluenesulfonamide |