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3-Acetyl-1-(4-methylphenyl)thiourea
The asymmetric unit of the title compound, C(10)H(12)N(2)OS, contains two independent molecules. In both molecules, the conformations of the two N—H bonds are anti to each other. Furthermore, the conformations of the amide C=S bonds and the C=O bonds are anti to each other. The dihedral angles bet...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393939/ https://www.ncbi.nlm.nih.gov/pubmed/22798804 http://dx.doi.org/10.1107/S1600536812026244 |
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author | Gowda, B. Thimme Foro, Sabine Kumar, Sharatha |
author_facet | Gowda, B. Thimme Foro, Sabine Kumar, Sharatha |
author_sort | Gowda, B. Thimme |
collection | PubMed |
description | The asymmetric unit of the title compound, C(10)H(12)N(2)OS, contains two independent molecules. In both molecules, the conformations of the two N—H bonds are anti to each other. Furthermore, the conformations of the amide C=S bonds and the C=O bonds are anti to each other. The dihedral angles between the benzene ring and the side chain are 52.8 (1) and 68.0 (1)° in the two independent molecules. An intramolecular N—H⋯O hydrogen bond occurs in both independent molecules. In the crystal, molecules are linked into infinite chains along the a axis through a series of N—H⋯O and N—H⋯S hydrogen bonds. |
format | Online Article Text |
id | pubmed-3393939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-33939392012-07-13 3-Acetyl-1-(4-methylphenyl)thiourea Gowda, B. Thimme Foro, Sabine Kumar, Sharatha Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(10)H(12)N(2)OS, contains two independent molecules. In both molecules, the conformations of the two N—H bonds are anti to each other. Furthermore, the conformations of the amide C=S bonds and the C=O bonds are anti to each other. The dihedral angles between the benzene ring and the side chain are 52.8 (1) and 68.0 (1)° in the two independent molecules. An intramolecular N—H⋯O hydrogen bond occurs in both independent molecules. In the crystal, molecules are linked into infinite chains along the a axis through a series of N—H⋯O and N—H⋯S hydrogen bonds. International Union of Crystallography 2012-06-16 /pmc/articles/PMC3393939/ /pubmed/22798804 http://dx.doi.org/10.1107/S1600536812026244 Text en © Gowda et al. 2012 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 Gowda, B. Thimme Foro, Sabine Kumar, Sharatha 3-Acetyl-1-(4-methylphenyl)thiourea |
title | 3-Acetyl-1-(4-methylphenyl)thiourea |
title_full | 3-Acetyl-1-(4-methylphenyl)thiourea |
title_fullStr | 3-Acetyl-1-(4-methylphenyl)thiourea |
title_full_unstemmed | 3-Acetyl-1-(4-methylphenyl)thiourea |
title_short | 3-Acetyl-1-(4-methylphenyl)thiourea |
title_sort | 3-acetyl-1-(4-methylphenyl)thiourea |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393939/ https://www.ncbi.nlm.nih.gov/pubmed/22798804 http://dx.doi.org/10.1107/S1600536812026244 |
work_keys_str_mv | AT gowdabthimme 3acetyl14methylphenylthiourea AT forosabine 3acetyl14methylphenylthiourea AT kumarsharatha 3acetyl14methylphenylthiourea |