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(E)-1-[2-(4-Chloro-2-nitro­styr­yl)-1-phenyl­sulfonyl-1H-indol-3-yl]propan-1-one

In the title compound, C(25)H(19)ClN(2)O(5)S, the phenyl ring forms dihedral angles of 79.62 (12) and 80.02 (13)° with the indole ring system and the benzene ring, respectively. The nitro group is twisted at an angle of 22.39 (11)° with respect to the attached benzene ring. In the crystal, mol­ecule...

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Autores principales: Umadevi, M., Saravanan, V., Yamuna, R., Mohanakrishnan, A. K., Chakkaravarthi, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004433/
https://www.ncbi.nlm.nih.gov/pubmed/24860289
http://dx.doi.org/10.1107/S1600536813031073
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author Umadevi, M.
Saravanan, V.
Yamuna, R.
Mohanakrishnan, A. K.
Chakkaravarthi, G.
author_facet Umadevi, M.
Saravanan, V.
Yamuna, R.
Mohanakrishnan, A. K.
Chakkaravarthi, G.
author_sort Umadevi, M.
collection PubMed
description In the title compound, C(25)H(19)ClN(2)O(5)S, the phenyl ring forms dihedral angles of 79.62 (12) and 80.02 (13)° with the indole ring system and the benzene ring, respectively. The nitro group is twisted at an angle of 22.39 (11)° with respect to the attached benzene ring. In the crystal, mol­ecules assemble into double layers in the ab plane via C—H⋯O inter­actions.
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spelling pubmed-40044332014-05-23 (E)-1-[2-(4-Chloro-2-nitro­styr­yl)-1-phenyl­sulfonyl-1H-indol-3-yl]propan-1-one Umadevi, M. Saravanan, V. Yamuna, R. Mohanakrishnan, A. K. Chakkaravarthi, G. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(25)H(19)ClN(2)O(5)S, the phenyl ring forms dihedral angles of 79.62 (12) and 80.02 (13)° with the indole ring system and the benzene ring, respectively. The nitro group is twisted at an angle of 22.39 (11)° with respect to the attached benzene ring. In the crystal, mol­ecules assemble into double layers in the ab plane via C—H⋯O inter­actions. International Union of Crystallography 2013-11-16 /pmc/articles/PMC4004433/ /pubmed/24860289 http://dx.doi.org/10.1107/S1600536813031073 Text en © Umadevi et al. 2013 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
Umadevi, M.
Saravanan, V.
Yamuna, R.
Mohanakrishnan, A. K.
Chakkaravarthi, G.
(E)-1-[2-(4-Chloro-2-nitro­styr­yl)-1-phenyl­sulfonyl-1H-indol-3-yl]propan-1-one
title (E)-1-[2-(4-Chloro-2-nitro­styr­yl)-1-phenyl­sulfonyl-1H-indol-3-yl]propan-1-one
title_full (E)-1-[2-(4-Chloro-2-nitro­styr­yl)-1-phenyl­sulfonyl-1H-indol-3-yl]propan-1-one
title_fullStr (E)-1-[2-(4-Chloro-2-nitro­styr­yl)-1-phenyl­sulfonyl-1H-indol-3-yl]propan-1-one
title_full_unstemmed (E)-1-[2-(4-Chloro-2-nitro­styr­yl)-1-phenyl­sulfonyl-1H-indol-3-yl]propan-1-one
title_short (E)-1-[2-(4-Chloro-2-nitro­styr­yl)-1-phenyl­sulfonyl-1H-indol-3-yl]propan-1-one
title_sort (e)-1-[2-(4-chloro-2-nitro­styr­yl)-1-phenyl­sulfonyl-1h-indol-3-yl]propan-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004433/
https://www.ncbi.nlm.nih.gov/pubmed/24860289
http://dx.doi.org/10.1107/S1600536813031073
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