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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.
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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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. |
format | Online Article Text |
id | pubmed-3470224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
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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