4-{[(E)-(3-Phenyl-1H-pyrazol-4-yl)methyl­idene]amino}-1H-1,2,4-triazole-5(4H)-thione

In the title compound, C(12)H(10)N(6)S, a weak intra­molecular C—H⋯S hydrogen bond stabilizes the mol­ecular conformation. The pyrazole and triazole rings form a dihedral angle of 17.82 (8)°. The mol­ecule adopts an E configuration with respect to the central C=N double bond. In the crystal, inter­m...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Hemamalini, Madhukar, Malladi, Shridhar, Isloor, Arun M.
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/PMC3212330/
https://www.ncbi.nlm.nih.gov/pubmed/22090987
http://dx.doi.org/10.1107/S1600536811024834
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author Fun, Hoong-Kun
Hemamalini, Madhukar
Malladi, Shridhar
Isloor, Arun M.
author_facet Fun, Hoong-Kun
Hemamalini, Madhukar
Malladi, Shridhar
Isloor, Arun M.
author_sort Fun, Hoong-Kun
collection PubMed
description In the title compound, C(12)H(10)N(6)S, a weak intra­molecular C—H⋯S hydrogen bond stabilizes the mol­ecular conformation. The pyrazole and triazole rings form a dihedral angle of 17.82 (8)°. The mol­ecule adopts an E configuration with respect to the central C=N double bond. In the crystal, inter­molecular N—H⋯N and N—H⋯S hydrogen bonds link mol­ecules into chains propagating in [20[Image: see text]].
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spelling pubmed-32123302011-11-16 4-{[(E)-(3-Phenyl-1H-pyrazol-4-yl)methyl­idene]amino}-1H-1,2,4-triazole-5(4H)-thione Fun, Hoong-Kun Hemamalini, Madhukar Malladi, Shridhar Isloor, Arun M. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(12)H(10)N(6)S, a weak intra­molecular C—H⋯S hydrogen bond stabilizes the mol­ecular conformation. The pyrazole and triazole rings form a dihedral angle of 17.82 (8)°. The mol­ecule adopts an E configuration with respect to the central C=N double bond. In the crystal, inter­molecular N—H⋯N and N—H⋯S hydrogen bonds link mol­ecules into chains propagating in [20[Image: see text]]. International Union of Crystallography 2011-07-09 /pmc/articles/PMC3212330/ /pubmed/22090987 http://dx.doi.org/10.1107/S1600536811024834 Text en © Fun et al. 2011 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
Fun, Hoong-Kun
Hemamalini, Madhukar
Malladi, Shridhar
Isloor, Arun M.
4-{[(E)-(3-Phenyl-1H-pyrazol-4-yl)methyl­idene]amino}-1H-1,2,4-triazole-5(4H)-thione
title 4-{[(E)-(3-Phenyl-1H-pyrazol-4-yl)methyl­idene]amino}-1H-1,2,4-triazole-5(4H)-thione
title_full 4-{[(E)-(3-Phenyl-1H-pyrazol-4-yl)methyl­idene]amino}-1H-1,2,4-triazole-5(4H)-thione
title_fullStr 4-{[(E)-(3-Phenyl-1H-pyrazol-4-yl)methyl­idene]amino}-1H-1,2,4-triazole-5(4H)-thione
title_full_unstemmed 4-{[(E)-(3-Phenyl-1H-pyrazol-4-yl)methyl­idene]amino}-1H-1,2,4-triazole-5(4H)-thione
title_short 4-{[(E)-(3-Phenyl-1H-pyrazol-4-yl)methyl­idene]amino}-1H-1,2,4-triazole-5(4H)-thione
title_sort 4-{[(e)-(3-phenyl-1h-pyrazol-4-yl)methyl­idene]amino}-1h-1,2,4-triazole-5(4h)-thione
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212330/
https://www.ncbi.nlm.nih.gov/pubmed/22090987
http://dx.doi.org/10.1107/S1600536811024834
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