3-Benzamidomethyl-4-[(E)-2-chloro­benzyl­ideneamino]-1H-1,2,4-triazole-5(4H)-thione

In the title compound, C(17)H(14)ClN(5)OS, the dihedral angles formed by the two benzene rings with the triazole ring are 66.88 (3) and 19.16 (3)°, and the benzene rings are inclined to each other with a dihedral angle of 78.40 (3)°. Inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into laye...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Jebas, Samuel Robinson, Rao, Jyothi N., Kalluraya, B.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2967963/
https://www.ncbi.nlm.nih.gov/pubmed/21581689
http://dx.doi.org/10.1107/S1600536808040361
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author Fun, Hoong-Kun
Jebas, Samuel Robinson
Rao, Jyothi N.
Kalluraya, B.
author_facet Fun, Hoong-Kun
Jebas, Samuel Robinson
Rao, Jyothi N.
Kalluraya, B.
author_sort Fun, Hoong-Kun
collection PubMed
description In the title compound, C(17)H(14)ClN(5)OS, the dihedral angles formed by the two benzene rings with the triazole ring are 66.88 (3) and 19.16 (3)°, and the benzene rings are inclined to each other with a dihedral angle of 78.40 (3)°. Inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into layers parallel to the (100) planes, and centrosymmetric π–π stacking inter­actions [centroid–centroid distance = 3.7717 (5) Å] are formed between benzene rings in neighbouring layers.
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spelling pubmed-29679632010-12-30 3-Benzamidomethyl-4-[(E)-2-chloro­benzyl­ideneamino]-1H-1,2,4-triazole-5(4H)-thione Fun, Hoong-Kun Jebas, Samuel Robinson Rao, Jyothi N. Kalluraya, B. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(17)H(14)ClN(5)OS, the dihedral angles formed by the two benzene rings with the triazole ring are 66.88 (3) and 19.16 (3)°, and the benzene rings are inclined to each other with a dihedral angle of 78.40 (3)°. Inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into layers parallel to the (100) planes, and centrosymmetric π–π stacking inter­actions [centroid–centroid distance = 3.7717 (5) Å] are formed between benzene rings in neighbouring layers. International Union of Crystallography 2008-12-10 /pmc/articles/PMC2967963/ /pubmed/21581689 http://dx.doi.org/10.1107/S1600536808040361 Text en © Fun et al. 2009 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
Jebas, Samuel Robinson
Rao, Jyothi N.
Kalluraya, B.
3-Benzamidomethyl-4-[(E)-2-chloro­benzyl­ideneamino]-1H-1,2,4-triazole-5(4H)-thione
title 3-Benzamidomethyl-4-[(E)-2-chloro­benzyl­ideneamino]-1H-1,2,4-triazole-5(4H)-thione
title_full 3-Benzamidomethyl-4-[(E)-2-chloro­benzyl­ideneamino]-1H-1,2,4-triazole-5(4H)-thione
title_fullStr 3-Benzamidomethyl-4-[(E)-2-chloro­benzyl­ideneamino]-1H-1,2,4-triazole-5(4H)-thione
title_full_unstemmed 3-Benzamidomethyl-4-[(E)-2-chloro­benzyl­ideneamino]-1H-1,2,4-triazole-5(4H)-thione
title_short 3-Benzamidomethyl-4-[(E)-2-chloro­benzyl­ideneamino]-1H-1,2,4-triazole-5(4H)-thione
title_sort 3-benzamidomethyl-4-[(e)-2-chloro­benzyl­ideneamino]-1h-1,2,4-triazole-5(4h)-thione
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2967963/
https://www.ncbi.nlm.nih.gov/pubmed/21581689
http://dx.doi.org/10.1107/S1600536808040361
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