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1,3-Dicyclo­hexyl-1-(4-nitro­benzo­yl)urea

In the title compound, C(20)H(27)N(3)O(4), both cyclo­hexane rings adopt chair conformations. The benzene ring and the amide group are oriented at a dihedral angle of 62.1 (2)°. In the crystal structure, inter­molecular N—H⋯O and C—H⋯O hydrogen bonds link the mol­ecules into chains propagating in [0...

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Detalles Bibliográficos
Autores principales: Dhinaa, A. N., Jagan, R., Sivakumar, K., Chinnakali, K.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979486/
https://www.ncbi.nlm.nih.gov/pubmed/21579388
http://dx.doi.org/10.1107/S1600536810016107
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author Dhinaa, A. N.
Jagan, R.
Sivakumar, K.
Chinnakali, K.
author_facet Dhinaa, A. N.
Jagan, R.
Sivakumar, K.
Chinnakali, K.
author_sort Dhinaa, A. N.
collection PubMed
description In the title compound, C(20)H(27)N(3)O(4), both cyclo­hexane rings adopt chair conformations. The benzene ring and the amide group are oriented at a dihedral angle of 62.1 (2)°. In the crystal structure, inter­molecular N—H⋯O and C—H⋯O hydrogen bonds link the mol­ecules into chains propagating in [010], which contain R (2) (2)(12) ring motifs.
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spelling pubmed-29794862010-12-30 1,3-Dicyclo­hexyl-1-(4-nitro­benzo­yl)urea Dhinaa, A. N. Jagan, R. Sivakumar, K. Chinnakali, K. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(20)H(27)N(3)O(4), both cyclo­hexane rings adopt chair conformations. The benzene ring and the amide group are oriented at a dihedral angle of 62.1 (2)°. In the crystal structure, inter­molecular N—H⋯O and C—H⋯O hydrogen bonds link the mol­ecules into chains propagating in [010], which contain R (2) (2)(12) ring motifs. International Union of Crystallography 2010-05-08 /pmc/articles/PMC2979486/ /pubmed/21579388 http://dx.doi.org/10.1107/S1600536810016107 Text en © Dhinaa et al. 2010 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
Dhinaa, A. N.
Jagan, R.
Sivakumar, K.
Chinnakali, K.
1,3-Dicyclo­hexyl-1-(4-nitro­benzo­yl)urea
title 1,3-Dicyclo­hexyl-1-(4-nitro­benzo­yl)urea
title_full 1,3-Dicyclo­hexyl-1-(4-nitro­benzo­yl)urea
title_fullStr 1,3-Dicyclo­hexyl-1-(4-nitro­benzo­yl)urea
title_full_unstemmed 1,3-Dicyclo­hexyl-1-(4-nitro­benzo­yl)urea
title_short 1,3-Dicyclo­hexyl-1-(4-nitro­benzo­yl)urea
title_sort 1,3-dicyclo­hexyl-1-(4-nitro­benzo­yl)urea
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979486/
https://www.ncbi.nlm.nih.gov/pubmed/21579388
http://dx.doi.org/10.1107/S1600536810016107
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