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1,3-Dicyclo­hexyl­imidazolidine-2,4,5-trione

The title compound, C(15)H(22)N(2)O(3), has been isolated as a by-product of an oxidative cleavage of the C—C bond linking two five-membered rings of 1,3-dicyclo­hexyl-5-(3-oxo-2,3-dihydro­benzofuran-2-yl)imidazolidine-2,4-dione. Individual mol­ecular units are engaged in weak C=O⋯C=O inter­actions...

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Detalles Bibliográficos
Autores principales: Talhi, Oualid, Fernandes, José A., Pinto, Diana C. G. A., Silva, Artur M. S., Almeida Paz, Filipe A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238900/
https://www.ncbi.nlm.nih.gov/pubmed/22199753
http://dx.doi.org/10.1107/S1600536811046253
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author Talhi, Oualid
Fernandes, José A.
Pinto, Diana C. G. A.
Silva, Artur M. S.
Almeida Paz, Filipe A.
author_facet Talhi, Oualid
Fernandes, José A.
Pinto, Diana C. G. A.
Silva, Artur M. S.
Almeida Paz, Filipe A.
author_sort Talhi, Oualid
collection PubMed
description The title compound, C(15)H(22)N(2)O(3), has been isolated as a by-product of an oxidative cleavage of the C—C bond linking two five-membered rings of 1,3-dicyclo­hexyl-5-(3-oxo-2,3-dihydro­benzofuran-2-yl)imidazolidine-2,4-dione. Individual mol­ecular units are engaged in weak C=O⋯C=O inter­actions [O⋯C = 2.814 (10) and 2.871 (11) Å], leading to the formation of supra­molecular chains which close pack, mediated by van der Waals contacts, in the bc plane.
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spelling pubmed-32389002011-12-23 1,3-Dicyclo­hexyl­imidazolidine-2,4,5-trione Talhi, Oualid Fernandes, José A. Pinto, Diana C. G. A. Silva, Artur M. S. Almeida Paz, Filipe A. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(15)H(22)N(2)O(3), has been isolated as a by-product of an oxidative cleavage of the C—C bond linking two five-membered rings of 1,3-dicyclo­hexyl-5-(3-oxo-2,3-dihydro­benzofuran-2-yl)imidazolidine-2,4-dione. Individual mol­ecular units are engaged in weak C=O⋯C=O inter­actions [O⋯C = 2.814 (10) and 2.871 (11) Å], leading to the formation of supra­molecular chains which close pack, mediated by van der Waals contacts, in the bc plane. International Union of Crystallography 2011-11-09 /pmc/articles/PMC3238900/ /pubmed/22199753 http://dx.doi.org/10.1107/S1600536811046253 Text en © Talhi 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
Talhi, Oualid
Fernandes, José A.
Pinto, Diana C. G. A.
Silva, Artur M. S.
Almeida Paz, Filipe A.
1,3-Dicyclo­hexyl­imidazolidine-2,4,5-trione
title 1,3-Dicyclo­hexyl­imidazolidine-2,4,5-trione
title_full 1,3-Dicyclo­hexyl­imidazolidine-2,4,5-trione
title_fullStr 1,3-Dicyclo­hexyl­imidazolidine-2,4,5-trione
title_full_unstemmed 1,3-Dicyclo­hexyl­imidazolidine-2,4,5-trione
title_short 1,3-Dicyclo­hexyl­imidazolidine-2,4,5-trione
title_sort 1,3-dicyclo­hexyl­imidazolidine-2,4,5-trione
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238900/
https://www.ncbi.nlm.nih.gov/pubmed/22199753
http://dx.doi.org/10.1107/S1600536811046253
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