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1-(2-Methylbenzoyl)-3-m-tolylthiourea
The molecule of the title compound, C(16)H(16)N(2)OS, is not planar; the two aromatic rings are inclined to one another by 37.59 (9)°. There are intramolecular hydrogen bonds between the benzoyl O atom and the H atom of the thioamide N atom, and between the thiourea S atom and the H atom of the t...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961788/ https://www.ncbi.nlm.nih.gov/pubmed/21202864 http://dx.doi.org/10.1107/S1600536808012300 |
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author | Yamin, B. M. Yousuf, S. Yusof, M. S. M. Zakaria, T. N. D. T. |
author_facet | Yamin, B. M. Yousuf, S. Yusof, M. S. M. Zakaria, T. N. D. T. |
author_sort | Yamin, B. M. |
collection | PubMed |
description | The molecule of the title compound, C(16)H(16)N(2)OS, is not planar; the two aromatic rings are inclined to one another by 37.59 (9)°. There are intramolecular hydrogen bonds between the benzoyl O atom and the H atom of the thioamide N atom, and between the thiourea S atom and the H atom of the tolyl group. These hydrogen bonds stabilize the molecule in such a way that the thiourea group adopts a trans–cis geometry. In the crystal structure, molecules are linked by N—H⋯S intermolecular hydrogen bonds, forming centrosymmetric dimers. |
format | Text |
id | pubmed-2961788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29617882010-12-30 1-(2-Methylbenzoyl)-3-m-tolylthiourea Yamin, B. M. Yousuf, S. Yusof, M. S. M. Zakaria, T. N. D. T. Acta Crystallogr Sect E Struct Rep Online Organic Papers The molecule of the title compound, C(16)H(16)N(2)OS, is not planar; the two aromatic rings are inclined to one another by 37.59 (9)°. There are intramolecular hydrogen bonds between the benzoyl O atom and the H atom of the thioamide N atom, and between the thiourea S atom and the H atom of the tolyl group. These hydrogen bonds stabilize the molecule in such a way that the thiourea group adopts a trans–cis geometry. In the crystal structure, molecules are linked by N—H⋯S intermolecular hydrogen bonds, forming centrosymmetric dimers. International Union of Crystallography 2008-06-07 /pmc/articles/PMC2961788/ /pubmed/21202864 http://dx.doi.org/10.1107/S1600536808012300 Text en © Yamin et al. 2008 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 Yamin, B. M. Yousuf, S. Yusof, M. S. M. Zakaria, T. N. D. T. 1-(2-Methylbenzoyl)-3-m-tolylthiourea |
title | 1-(2-Methylbenzoyl)-3-m-tolylthiourea |
title_full | 1-(2-Methylbenzoyl)-3-m-tolylthiourea |
title_fullStr | 1-(2-Methylbenzoyl)-3-m-tolylthiourea |
title_full_unstemmed | 1-(2-Methylbenzoyl)-3-m-tolylthiourea |
title_short | 1-(2-Methylbenzoyl)-3-m-tolylthiourea |
title_sort | 1-(2-methylbenzoyl)-3-m-tolylthiourea |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961788/ https://www.ncbi.nlm.nih.gov/pubmed/21202864 http://dx.doi.org/10.1107/S1600536808012300 |
work_keys_str_mv | AT yaminbm 12methylbenzoyl3mtolylthiourea AT yousufs 12methylbenzoyl3mtolylthiourea AT yusofmsm 12methylbenzoyl3mtolylthiourea AT zakariatndt 12methylbenzoyl3mtolylthiourea |