1,5-Bis(4-iso­propyl­benzyl­idene)thio­carbonohydrazide

The title compound, C(21)H(26)N(4)S, was synthesized by the condensation reaction of 4-iso­propyl­benzaldehyde with thio­carbohydrazide in ethanol. The planes of the two benzene rings in the mol­ecule are inclined at 22.6 (1)°. In the crystal, pairs of inter­molecular N—H⋯S hydrogen bonds link the m...

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Detalles Bibliográficos
Autores principales: Han, Yan-Hua, Zhao, Qiao, Wang, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884323/
https://www.ncbi.nlm.nih.gov/pubmed/24454099
http://dx.doi.org/10.1107/S1600536813027293
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author Han, Yan-Hua
Zhao, Qiao
Wang, Yong
author_facet Han, Yan-Hua
Zhao, Qiao
Wang, Yong
author_sort Han, Yan-Hua
collection PubMed
description The title compound, C(21)H(26)N(4)S, was synthesized by the condensation reaction of 4-iso­propyl­benzaldehyde with thio­carbohydrazide in ethanol. The planes of the two benzene rings in the mol­ecule are inclined at 22.6 (1)°. In the crystal, pairs of inter­molecular N—H⋯S hydrogen bonds link the mol­ecules into inversion dimers.
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spelling pubmed-38843232014-01-17 1,5-Bis(4-iso­propyl­benzyl­idene)thio­carbonohydrazide Han, Yan-Hua Zhao, Qiao Wang, Yong Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(21)H(26)N(4)S, was synthesized by the condensation reaction of 4-iso­propyl­benzaldehyde with thio­carbohydrazide in ethanol. The planes of the two benzene rings in the mol­ecule are inclined at 22.6 (1)°. In the crystal, pairs of inter­molecular N—H⋯S hydrogen bonds link the mol­ecules into inversion dimers. International Union of Crystallography 2013-10-19 /pmc/articles/PMC3884323/ /pubmed/24454099 http://dx.doi.org/10.1107/S1600536813027293 Text en © Han et al. 2013 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
Han, Yan-Hua
Zhao, Qiao
Wang, Yong
1,5-Bis(4-iso­propyl­benzyl­idene)thio­carbonohydrazide
title 1,5-Bis(4-iso­propyl­benzyl­idene)thio­carbonohydrazide
title_full 1,5-Bis(4-iso­propyl­benzyl­idene)thio­carbonohydrazide
title_fullStr 1,5-Bis(4-iso­propyl­benzyl­idene)thio­carbonohydrazide
title_full_unstemmed 1,5-Bis(4-iso­propyl­benzyl­idene)thio­carbonohydrazide
title_short 1,5-Bis(4-iso­propyl­benzyl­idene)thio­carbonohydrazide
title_sort 1,5-bis(4-iso­propyl­benzyl­idene)thio­carbonohydrazide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884323/
https://www.ncbi.nlm.nih.gov/pubmed/24454099
http://dx.doi.org/10.1107/S1600536813027293
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AT zhaoqiao 15bis4isopropylbenzylidenethiocarbonohydrazide
AT wangyong 15bis4isopropylbenzylidenethiocarbonohydrazide

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