N-Benzyl­carbamothioyl-2-chloro­benzamide

In the title compound, C(15)H(13)ClN(2)OS, the dihedral angles between the sulfourea group and the benzene ring and the chloro­benzene ring are 35.8 (6) and 81.6 (6)° respectively. An intra­molecular N—H⋯O inter­action occurs. In the crystal, a combination of inter­molecular π–π stacking inter­actio...

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Detalles Bibliográficos
Autores principales: Zheng, Xi, Li, Bo, Wang, Qiang, Guo, Li
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006700/
https://www.ncbi.nlm.nih.gov/pubmed/21587987
http://dx.doi.org/10.1107/S1600536810023822
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author Zheng, Xi
Li, Bo
Wang, Qiang
Guo, Li
author_facet Zheng, Xi
Li, Bo
Wang, Qiang
Guo, Li
author_sort Zheng, Xi
collection PubMed
description In the title compound, C(15)H(13)ClN(2)OS, the dihedral angles between the sulfourea group and the benzene ring and the chloro­benzene ring are 35.8 (6) and 81.6 (6)° respectively. An intra­molecular N—H⋯O inter­action occurs. In the crystal, a combination of inter­molecular π–π stacking inter­actions [centroid–centroid distance = 4.0616 (16) Å] and N—H⋯S hydrogen bonds stabilizes the structure.
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spelling pubmed-30067002010-12-30 N-Benzyl­carbamothioyl-2-chloro­benzamide Zheng, Xi Li, Bo Wang, Qiang Guo, Li Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(13)ClN(2)OS, the dihedral angles between the sulfourea group and the benzene ring and the chloro­benzene ring are 35.8 (6) and 81.6 (6)° respectively. An intra­molecular N—H⋯O inter­action occurs. In the crystal, a combination of inter­molecular π–π stacking inter­actions [centroid–centroid distance = 4.0616 (16) Å] and N—H⋯S hydrogen bonds stabilizes the structure. International Union of Crystallography 2010-06-26 /pmc/articles/PMC3006700/ /pubmed/21587987 http://dx.doi.org/10.1107/S1600536810023822 Text en © Zheng et al. 2010 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
Zheng, Xi
Li, Bo
Wang, Qiang
Guo, Li
N-Benzyl­carbamothioyl-2-chloro­benzamide
title N-Benzyl­carbamothioyl-2-chloro­benzamide
title_full N-Benzyl­carbamothioyl-2-chloro­benzamide
title_fullStr N-Benzyl­carbamothioyl-2-chloro­benzamide
title_full_unstemmed N-Benzyl­carbamothioyl-2-chloro­benzamide
title_short N-Benzyl­carbamothioyl-2-chloro­benzamide
title_sort n-benzyl­carbamothioyl-2-chloro­benzamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006700/
https://www.ncbi.nlm.nih.gov/pubmed/21587987
http://dx.doi.org/10.1107/S1600536810023822
work_keys_str_mv AT zhengxi nbenzylcarbamothioyl2chlorobenzamide
AT libo nbenzylcarbamothioyl2chlorobenzamide
AT wangqiang nbenzylcarbamothioyl2chlorobenzamide
AT guoli nbenzylcarbamothioyl2chlorobenzamide

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