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(Z)-N-Ethyl-2-(5-fluoro-2-oxoindolin-3-yl­idene)hydrazinecarbothio­amide

In the title compound, C(11)H(11)FN(4)OS, an intra­molecular N—H⋯O hydrogen bond generates an S(6) ring. In the crystal, mol­ecules form chains through N—H⋯O hydrogen bonds, which are extended by N—H⋯S hydrogen bonds into an infinite three-dimensional network.

Detalles Bibliográficos
Autores principales: Ali, Amna Qasem, Eltayeb, Naser Eltaher, Teoh, Siang Guan, Salhin, Abdussalam, Fun, Hoong-Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3470224/
https://www.ncbi.nlm.nih.gov/pubmed/23125668
http://dx.doi.org/10.1107/S1600536812036471
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author Ali, Amna Qasem
Eltayeb, Naser Eltaher
Teoh, Siang Guan
Salhin, Abdussalam
Fun, Hoong-Kun
author_facet Ali, Amna Qasem
Eltayeb, Naser Eltaher
Teoh, Siang Guan
Salhin, Abdussalam
Fun, Hoong-Kun
author_sort Ali, Amna Qasem
collection PubMed
description In the title compound, C(11)H(11)FN(4)OS, an intra­molecular N—H⋯O hydrogen bond generates an S(6) ring. In the crystal, mol­ecules form chains through N—H⋯O hydrogen bonds, which are extended by N—H⋯S hydrogen bonds into an infinite three-dimensional network.
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spelling pubmed-34702242012-11-02 (Z)-N-Ethyl-2-(5-fluoro-2-oxoindolin-3-yl­idene)hydrazinecarbothio­amide Ali, Amna Qasem Eltayeb, Naser Eltaher Teoh, Siang Guan Salhin, Abdussalam Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(11)H(11)FN(4)OS, an intra­molecular N—H⋯O hydrogen bond generates an S(6) ring. In the crystal, mol­ecules form chains through N—H⋯O hydrogen bonds, which are extended by N—H⋯S hydrogen bonds into an infinite three-dimensional network. International Union of Crystallography 2012-09-08 /pmc/articles/PMC3470224/ /pubmed/23125668 http://dx.doi.org/10.1107/S1600536812036471 Text en © Ali 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
Ali, Amna Qasem
Eltayeb, Naser Eltaher
Teoh, Siang Guan
Salhin, Abdussalam
Fun, Hoong-Kun
(Z)-N-Ethyl-2-(5-fluoro-2-oxoindolin-3-yl­idene)hydrazinecarbothio­amide
title (Z)-N-Ethyl-2-(5-fluoro-2-oxoindolin-3-yl­idene)hydrazinecarbothio­amide
title_full (Z)-N-Ethyl-2-(5-fluoro-2-oxoindolin-3-yl­idene)hydrazinecarbothio­amide
title_fullStr (Z)-N-Ethyl-2-(5-fluoro-2-oxoindolin-3-yl­idene)hydrazinecarbothio­amide
title_full_unstemmed (Z)-N-Ethyl-2-(5-fluoro-2-oxoindolin-3-yl­idene)hydrazinecarbothio­amide
title_short (Z)-N-Ethyl-2-(5-fluoro-2-oxoindolin-3-yl­idene)hydrazinecarbothio­amide
title_sort (z)-n-ethyl-2-(5-fluoro-2-oxoindolin-3-yl­idene)hydrazinecarbothio­amide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3470224/
https://www.ncbi.nlm.nih.gov/pubmed/23125668
http://dx.doi.org/10.1107/S1600536812036471
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