(E)-2-[(E)-3-(Hy­droxy­imino)­butan-2-yl­idene]-N-methyl­hydrazinecarbothio­amide

In the title compound, C(6)H(12)N(4)OS, an intra­molecular N—H⋯N hydrogen-bond is present giving rise to an S(5) ring motif. In the crystal, double-stranded chains propagating along [10[Image: see text]] are formed via pairs of O—H⋯S and N—H⋯S hydrogen bonds. The chains are further stabilized by C—H...

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Detalles Bibliográficos
Autores principales: Abduelftah, Halema Shaban, Ali, Amna Qasem, Eltayeb, Naser Eltaher, Teoh, Siang Guan, Fun, Hoong-Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3254522/
https://www.ncbi.nlm.nih.gov/pubmed/22259468
http://dx.doi.org/10.1107/S1600536811053621
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author Abduelftah, Halema Shaban
Ali, Amna Qasem
Eltayeb, Naser Eltaher
Teoh, Siang Guan
Fun, Hoong-Kun
author_facet Abduelftah, Halema Shaban
Ali, Amna Qasem
Eltayeb, Naser Eltaher
Teoh, Siang Guan
Fun, Hoong-Kun
author_sort Abduelftah, Halema Shaban
collection PubMed
description In the title compound, C(6)H(12)N(4)OS, an intra­molecular N—H⋯N hydrogen-bond is present giving rise to an S(5) ring motif. In the crystal, double-stranded chains propagating along [10[Image: see text]] are formed via pairs of O—H⋯S and N—H⋯S hydrogen bonds. The chains are further stabilized by C—H⋯S interactions.
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spelling pubmed-32545222012-01-18 (E)-2-[(E)-3-(Hy­droxy­imino)­butan-2-yl­idene]-N-methyl­hydrazinecarbothio­amide Abduelftah, Halema Shaban Ali, Amna Qasem Eltayeb, Naser Eltaher Teoh, Siang Guan Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(6)H(12)N(4)OS, an intra­molecular N—H⋯N hydrogen-bond is present giving rise to an S(5) ring motif. In the crystal, double-stranded chains propagating along [10[Image: see text]] are formed via pairs of O—H⋯S and N—H⋯S hydrogen bonds. The chains are further stabilized by C—H⋯S interactions. International Union of Crystallography 2011-12-21 /pmc/articles/PMC3254522/ /pubmed/22259468 http://dx.doi.org/10.1107/S1600536811053621 Text en © Abduelftah 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
Abduelftah, Halema Shaban
Ali, Amna Qasem
Eltayeb, Naser Eltaher
Teoh, Siang Guan
Fun, Hoong-Kun
(E)-2-[(E)-3-(Hy­droxy­imino)­butan-2-yl­idene]-N-methyl­hydrazinecarbothio­amide
title (E)-2-[(E)-3-(Hy­droxy­imino)­butan-2-yl­idene]-N-methyl­hydrazinecarbothio­amide
title_full (E)-2-[(E)-3-(Hy­droxy­imino)­butan-2-yl­idene]-N-methyl­hydrazinecarbothio­amide
title_fullStr (E)-2-[(E)-3-(Hy­droxy­imino)­butan-2-yl­idene]-N-methyl­hydrazinecarbothio­amide
title_full_unstemmed (E)-2-[(E)-3-(Hy­droxy­imino)­butan-2-yl­idene]-N-methyl­hydrazinecarbothio­amide
title_short (E)-2-[(E)-3-(Hy­droxy­imino)­butan-2-yl­idene]-N-methyl­hydrazinecarbothio­amide
title_sort (e)-2-[(e)-3-(hy­droxy­imino)­butan-2-yl­idene]-n-methyl­hydrazinecarbothio­amide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3254522/
https://www.ncbi.nlm.nih.gov/pubmed/22259468
http://dx.doi.org/10.1107/S1600536811053621
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