3-Cyclo­hexyl­sulfan­yl-2-(4-methyl­phen­yl)-5,7-dinitro-1H-indole

In the title compound, C(21)H(21)N(3)O(4)S, the cyclo­hexane ring adopts a chair conformation. The nitro and methyl­phenyl groups are all coplanar with the indole ring system. Intra­molecular N—H⋯O and C—H⋯S hydrogen bonds generate S(6) ring motifs. The mol­ecules form R (2) (2)(20) centrosymmetric...

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Detalles Bibliográficos
Autores principales: Ramesh, P., Subbiahpandi, A., Manikannan, Ramaiyan, Muthusubramanian, S., Ponnuswamy, M. N.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959479/
https://www.ncbi.nlm.nih.gov/pubmed/21201102
http://dx.doi.org/10.1107/S1600536808027682
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author Ramesh, P.
Subbiahpandi, A.
Manikannan, Ramaiyan
Muthusubramanian, S.
Ponnuswamy, M. N.
author_facet Ramesh, P.
Subbiahpandi, A.
Manikannan, Ramaiyan
Muthusubramanian, S.
Ponnuswamy, M. N.
author_sort Ramesh, P.
collection PubMed
description In the title compound, C(21)H(21)N(3)O(4)S, the cyclo­hexane ring adopts a chair conformation. The nitro and methyl­phenyl groups are all coplanar with the indole ring system. Intra­molecular N—H⋯O and C—H⋯S hydrogen bonds generate S(6) ring motifs. The mol­ecules form R (2) (2)(20) centrosymmetric dimers via inter­molecular C—H⋯O hydrogen bonds. A short O⋯O contact [2.842 (2) Å] is observed in the dimer.
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spelling pubmed-29594792010-12-30 3-Cyclo­hexyl­sulfan­yl-2-(4-methyl­phen­yl)-5,7-dinitro-1H-indole Ramesh, P. Subbiahpandi, A. Manikannan, Ramaiyan Muthusubramanian, S. Ponnuswamy, M. N. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(21)H(21)N(3)O(4)S, the cyclo­hexane ring adopts a chair conformation. The nitro and methyl­phenyl groups are all coplanar with the indole ring system. Intra­molecular N—H⋯O and C—H⋯S hydrogen bonds generate S(6) ring motifs. The mol­ecules form R (2) (2)(20) centrosymmetric dimers via inter­molecular C—H⋯O hydrogen bonds. A short O⋯O contact [2.842 (2) Å] is observed in the dimer. International Union of Crystallography 2008-09-06 /pmc/articles/PMC2959479/ /pubmed/21201102 http://dx.doi.org/10.1107/S1600536808027682 Text en © Ramesh et al. 2008 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
Ramesh, P.
Subbiahpandi, A.
Manikannan, Ramaiyan
Muthusubramanian, S.
Ponnuswamy, M. N.
3-Cyclo­hexyl­sulfan­yl-2-(4-methyl­phen­yl)-5,7-dinitro-1H-indole
title 3-Cyclo­hexyl­sulfan­yl-2-(4-methyl­phen­yl)-5,7-dinitro-1H-indole
title_full 3-Cyclo­hexyl­sulfan­yl-2-(4-methyl­phen­yl)-5,7-dinitro-1H-indole
title_fullStr 3-Cyclo­hexyl­sulfan­yl-2-(4-methyl­phen­yl)-5,7-dinitro-1H-indole
title_full_unstemmed 3-Cyclo­hexyl­sulfan­yl-2-(4-methyl­phen­yl)-5,7-dinitro-1H-indole
title_short 3-Cyclo­hexyl­sulfan­yl-2-(4-methyl­phen­yl)-5,7-dinitro-1H-indole
title_sort 3-cyclo­hexyl­sulfan­yl-2-(4-methyl­phen­yl)-5,7-dinitro-1h-indole
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959479/
https://www.ncbi.nlm.nih.gov/pubmed/21201102
http://dx.doi.org/10.1107/S1600536808027682
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