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1-Benzylideneamino-3-(4-methylphenyl)thiourea
In the title compound, C(15)H(15)N(3)S, the almost planar 2-benzylidenehydrazinecarbothioamide unit (r.m.s. deviation = 0.0351 Å) is aligned at a dihedral angle of 64.42 (6)° with respect to the plane of the tolyl ring. The molecule exhibits an E configuration for the azomethine linkage. In the c...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051669/ https://www.ncbi.nlm.nih.gov/pubmed/21523112 http://dx.doi.org/10.1107/S160053681100198X |
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author | Zhang, Yan-Ling Xu, Zhi-Hong Zhang, Fu-Juan Yang, Feng-Ling |
author_facet | Zhang, Yan-Ling Xu, Zhi-Hong Zhang, Fu-Juan Yang, Feng-Ling |
author_sort | Zhang, Yan-Ling |
collection | PubMed |
description | In the title compound, C(15)H(15)N(3)S, the almost planar 2-benzylidenehydrazinecarbothioamide unit (r.m.s. deviation = 0.0351 Å) is aligned at a dihedral angle of 64.42 (6)° with respect to the plane of the tolyl ring. The molecule exhibits an E configuration for the azomethine linkage. In the crystal, intermolecular N—H⋯S hydrogen bonds about centers of inversion lead to the formation of dimers. |
format | Text |
id | pubmed-3051669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30516692011-04-26 1-Benzylideneamino-3-(4-methylphenyl)thiourea Zhang, Yan-Ling Xu, Zhi-Hong Zhang, Fu-Juan Yang, Feng-Ling Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(15)N(3)S, the almost planar 2-benzylidenehydrazinecarbothioamide unit (r.m.s. deviation = 0.0351 Å) is aligned at a dihedral angle of 64.42 (6)° with respect to the plane of the tolyl ring. The molecule exhibits an E configuration for the azomethine linkage. In the crystal, intermolecular N—H⋯S hydrogen bonds about centers of inversion lead to the formation of dimers. International Union of Crystallography 2011-01-22 /pmc/articles/PMC3051669/ /pubmed/21523112 http://dx.doi.org/10.1107/S160053681100198X Text en © Zhang 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 Zhang, Yan-Ling Xu, Zhi-Hong Zhang, Fu-Juan Yang, Feng-Ling 1-Benzylideneamino-3-(4-methylphenyl)thiourea |
title | 1-Benzylideneamino-3-(4-methylphenyl)thiourea |
title_full | 1-Benzylideneamino-3-(4-methylphenyl)thiourea |
title_fullStr | 1-Benzylideneamino-3-(4-methylphenyl)thiourea |
title_full_unstemmed | 1-Benzylideneamino-3-(4-methylphenyl)thiourea |
title_short | 1-Benzylideneamino-3-(4-methylphenyl)thiourea |
title_sort | 1-benzylideneamino-3-(4-methylphenyl)thiourea |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051669/ https://www.ncbi.nlm.nih.gov/pubmed/21523112 http://dx.doi.org/10.1107/S160053681100198X |
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