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(Z)-N-Methyl-2-(5-nitro-2-oxoindolin-3-yl­idene)hydrazinecarbothio­amide

In the title compound, C(10)H(9)N(5)O(3)S, an intra­molecular N—H⋯O hydrogen bond generates an S(6) ring motif. In the crystal, mol­ecules are linked via N—H⋯S hydrogen bonds into a zigzag chain along the b axis. C—H⋯O inter­actions are observed between the chains.

Detalles Bibliográficos
Autores principales: Qasem Ali, Amna, 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/PMC3343934/
https://www.ncbi.nlm.nih.gov/pubmed/22590015
http://dx.doi.org/10.1107/S1600536812001183
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author Qasem Ali, Amna
Eltayeb, Naser Eltaher
Teoh, Siang Guan
Salhin, Abdussalam
Fun, Hoong-Kun
author_facet Qasem Ali, Amna
Eltayeb, Naser Eltaher
Teoh, Siang Guan
Salhin, Abdussalam
Fun, Hoong-Kun
author_sort Qasem Ali, Amna
collection PubMed
description In the title compound, C(10)H(9)N(5)O(3)S, an intra­molecular N—H⋯O hydrogen bond generates an S(6) ring motif. In the crystal, mol­ecules are linked via N—H⋯S hydrogen bonds into a zigzag chain along the b axis. C—H⋯O inter­actions are observed between the chains.
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spelling pubmed-33439342012-05-15 (Z)-N-Methyl-2-(5-nitro-2-oxoindolin-3-yl­idene)hydrazinecarbothio­amide Qasem Ali, Amna 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(10)H(9)N(5)O(3)S, an intra­molecular N—H⋯O hydrogen bond generates an S(6) ring motif. In the crystal, mol­ecules are linked via N—H⋯S hydrogen bonds into a zigzag chain along the b axis. C—H⋯O inter­actions are observed between the chains. International Union of Crystallography 2012-03-03 /pmc/articles/PMC3343934/ /pubmed/22590015 http://dx.doi.org/10.1107/S1600536812001183 Text en © Qasem 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
Qasem Ali, Amna
Eltayeb, Naser Eltaher
Teoh, Siang Guan
Salhin, Abdussalam
Fun, Hoong-Kun
(Z)-N-Methyl-2-(5-nitro-2-oxoindolin-3-yl­idene)hydrazinecarbothio­amide
title (Z)-N-Methyl-2-(5-nitro-2-oxoindolin-3-yl­idene)hydrazinecarbothio­amide
title_full (Z)-N-Methyl-2-(5-nitro-2-oxoindolin-3-yl­idene)hydrazinecarbothio­amide
title_fullStr (Z)-N-Methyl-2-(5-nitro-2-oxoindolin-3-yl­idene)hydrazinecarbothio­amide
title_full_unstemmed (Z)-N-Methyl-2-(5-nitro-2-oxoindolin-3-yl­idene)hydrazinecarbothio­amide
title_short (Z)-N-Methyl-2-(5-nitro-2-oxoindolin-3-yl­idene)hydrazinecarbothio­amide
title_sort (z)-n-methyl-2-(5-nitro-2-oxoindolin-3-yl­idene)hydrazinecarbothio­amide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3343934/
https://www.ncbi.nlm.nih.gov/pubmed/22590015
http://dx.doi.org/10.1107/S1600536812001183
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