1,3-Bis(1-cyclo­hexyl­eth­yl)imidazolidine-2-thione

The complete mol­ecule of the title compound, C(19)H(34)N(2)S, is generated by crystallographic twofold symmetry, with the C=S group lying on the rotation axis. A short C—H⋯S contact occurs in the mol­ecule. The five-membered ring is twisted and the cyclo­hexyl ring adopts a chair conformation. The...

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Detalles Bibliográficos
Autores principales: Umar, M. Naveed, Tahir, M. Nawaz, Shoaib, Mohammad, Ali, Akbar, Ziauddin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295511/
https://www.ncbi.nlm.nih.gov/pubmed/22412622
http://dx.doi.org/10.1107/S1600536812006150
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author Umar, M. Naveed
Tahir, M. Nawaz
Shoaib, Mohammad
Ali, Akbar
Ziauddin,
author_facet Umar, M. Naveed
Tahir, M. Nawaz
Shoaib, Mohammad
Ali, Akbar
Ziauddin,
author_sort Umar, M. Naveed
collection PubMed
description The complete mol­ecule of the title compound, C(19)H(34)N(2)S, is generated by crystallographic twofold symmetry, with the C=S group lying on the rotation axis. A short C—H⋯S contact occurs in the mol­ecule. The five-membered ring is twisted and the cyclo­hexyl ring adopts a chair conformation. The dihedral angle between the mean plane of the five-membered ring and the basal plane of the cyclo­hexyl ring is 75.32 (13)°.
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spelling pubmed-32955112012-03-12 1,3-Bis(1-cyclo­hexyl­eth­yl)imidazolidine-2-thione Umar, M. Naveed Tahir, M. Nawaz Shoaib, Mohammad Ali, Akbar Ziauddin, Acta Crystallogr Sect E Struct Rep Online Organic Papers The complete mol­ecule of the title compound, C(19)H(34)N(2)S, is generated by crystallographic twofold symmetry, with the C=S group lying on the rotation axis. A short C—H⋯S contact occurs in the mol­ecule. The five-membered ring is twisted and the cyclo­hexyl ring adopts a chair conformation. The dihedral angle between the mean plane of the five-membered ring and the basal plane of the cyclo­hexyl ring is 75.32 (13)°. International Union of Crystallography 2012-02-17 /pmc/articles/PMC3295511/ /pubmed/22412622 http://dx.doi.org/10.1107/S1600536812006150 Text en © Umar 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
Umar, M. Naveed
Tahir, M. Nawaz
Shoaib, Mohammad
Ali, Akbar
Ziauddin,
1,3-Bis(1-cyclo­hexyl­eth­yl)imidazolidine-2-thione
title 1,3-Bis(1-cyclo­hexyl­eth­yl)imidazolidine-2-thione
title_full 1,3-Bis(1-cyclo­hexyl­eth­yl)imidazolidine-2-thione
title_fullStr 1,3-Bis(1-cyclo­hexyl­eth­yl)imidazolidine-2-thione
title_full_unstemmed 1,3-Bis(1-cyclo­hexyl­eth­yl)imidazolidine-2-thione
title_short 1,3-Bis(1-cyclo­hexyl­eth­yl)imidazolidine-2-thione
title_sort 1,3-bis(1-cyclo­hexyl­eth­yl)imidazolidine-2-thione
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295511/
https://www.ncbi.nlm.nih.gov/pubmed/22412622
http://dx.doi.org/10.1107/S1600536812006150
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