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3-Chloro-N-[N-(furan-2-carbonyl)hydrazinocarbothioyl]benzamide
In the title compound C(13)H(10)ClN(3)O(3)S, the benzoyl group maintains its trans conformation against the thiono group about the C—N bond and the intramolecular hydrogen bond between the benzoyl O atom and thioamide H atom. In the crystal, N—H⋯O and C—H⋯O hydrogen bonds link the molecules, form...
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/PMC3790427/ https://www.ncbi.nlm.nih.gov/pubmed/24098246 http://dx.doi.org/10.1107/S1600536813025440 |
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author | Yamin, Bohari M Yusof, Diyana Hasbullah, Siti Aishah |
author_facet | Yamin, Bohari M Yusof, Diyana Hasbullah, Siti Aishah |
author_sort | Yamin, Bohari M |
collection | PubMed |
description | In the title compound C(13)H(10)ClN(3)O(3)S, the benzoyl group maintains its trans conformation against the thiono group about the C—N bond and the intramolecular hydrogen bond between the benzoyl O atom and thioamide H atom. In the crystal, N—H⋯O and C—H⋯O hydrogen bonds link the molecules, forming chains along the b-axis direction. In addition, C—H⋯π interactions occur between a phenyl H atom and the furan ring. |
format | Online Article Text |
id | pubmed-3790427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-37904272013-10-04 3-Chloro-N-[N-(furan-2-carbonyl)hydrazinocarbothioyl]benzamide Yamin, Bohari M Yusof, Diyana Hasbullah, Siti Aishah Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound C(13)H(10)ClN(3)O(3)S, the benzoyl group maintains its trans conformation against the thiono group about the C—N bond and the intramolecular hydrogen bond between the benzoyl O atom and thioamide H atom. In the crystal, N—H⋯O and C—H⋯O hydrogen bonds link the molecules, forming chains along the b-axis direction. In addition, C—H⋯π interactions occur between a phenyl H atom and the furan ring. International Union of Crystallography 2013-09-21 /pmc/articles/PMC3790427/ /pubmed/24098246 http://dx.doi.org/10.1107/S1600536813025440 Text en © Yamin 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 Yamin, Bohari M Yusof, Diyana Hasbullah, Siti Aishah 3-Chloro-N-[N-(furan-2-carbonyl)hydrazinocarbothioyl]benzamide |
title | 3-Chloro-N-[N-(furan-2-carbonyl)hydrazinocarbothioyl]benzamide |
title_full | 3-Chloro-N-[N-(furan-2-carbonyl)hydrazinocarbothioyl]benzamide |
title_fullStr | 3-Chloro-N-[N-(furan-2-carbonyl)hydrazinocarbothioyl]benzamide |
title_full_unstemmed | 3-Chloro-N-[N-(furan-2-carbonyl)hydrazinocarbothioyl]benzamide |
title_short | 3-Chloro-N-[N-(furan-2-carbonyl)hydrazinocarbothioyl]benzamide |
title_sort | 3-chloro-n-[n-(furan-2-carbonyl)hydrazinocarbothioyl]benzamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790427/ https://www.ncbi.nlm.nih.gov/pubmed/24098246 http://dx.doi.org/10.1107/S1600536813025440 |
work_keys_str_mv | AT yaminboharim 3chloronnfuran2carbonylhydrazinocarbothioylbenzamide AT yusofdiyana 3chloronnfuran2carbonylhydrazinocarbothioylbenzamide AT hasbullahsitiaishah 3chloronnfuran2carbonylhydrazinocarbothioylbenzamide |