Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Yamin, Bohari M, Yusof, Diyana, Hasbullah, Siti Aishah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
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
_version_ 1782286594997223424
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