(Phen­yl)(1-phenyl­sulfonyl-1H-indol-3-yl)methanone

In the title compound, C(21)H(15)NO(3)S, the sulfonyl-bound phenyl ring forms a dihedral angle of 86.28 (5)° with the indole ring system. The mol­ecular structure is stabilized by intra­molecular C—H⋯O hydrogen bonds. The crystal packing is stabilized by weak inter­molecular C—H⋯O and C—H⋯π inter­ac...

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Detalles Bibliográficos
Autores principales: Chakkaravarthi, G., Panchatcharam, R., Dhayalan, V., Mohanakrishnan, A. K., Manivannan, V.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009149/
https://www.ncbi.nlm.nih.gov/pubmed/21589073
http://dx.doi.org/10.1107/S1600536810042261
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author Chakkaravarthi, G.
Panchatcharam, R.
Dhayalan, V.
Mohanakrishnan, A. K.
Manivannan, V.
author_facet Chakkaravarthi, G.
Panchatcharam, R.
Dhayalan, V.
Mohanakrishnan, A. K.
Manivannan, V.
author_sort Chakkaravarthi, G.
collection PubMed
description In the title compound, C(21)H(15)NO(3)S, the sulfonyl-bound phenyl ring forms a dihedral angle of 86.28 (5)° with the indole ring system. The mol­ecular structure is stabilized by intra­molecular C—H⋯O hydrogen bonds. The crystal packing is stabilized by weak inter­molecular C—H⋯O and C—H⋯π inter­actions.
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spelling pubmed-30091492010-12-30 (Phen­yl)(1-phenyl­sulfonyl-1H-indol-3-yl)methanone Chakkaravarthi, G. Panchatcharam, R. Dhayalan, V. Mohanakrishnan, A. K. Manivannan, V. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(21)H(15)NO(3)S, the sulfonyl-bound phenyl ring forms a dihedral angle of 86.28 (5)° with the indole ring system. The mol­ecular structure is stabilized by intra­molecular C—H⋯O hydrogen bonds. The crystal packing is stabilized by weak inter­molecular C—H⋯O and C—H⋯π inter­actions. International Union of Crystallography 2010-10-23 /pmc/articles/PMC3009149/ /pubmed/21589073 http://dx.doi.org/10.1107/S1600536810042261 Text en © Chakkaravarthi 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
Chakkaravarthi, G.
Panchatcharam, R.
Dhayalan, V.
Mohanakrishnan, A. K.
Manivannan, V.
(Phen­yl)(1-phenyl­sulfonyl-1H-indol-3-yl)methanone
title (Phen­yl)(1-phenyl­sulfonyl-1H-indol-3-yl)methanone
title_full (Phen­yl)(1-phenyl­sulfonyl-1H-indol-3-yl)methanone
title_fullStr (Phen­yl)(1-phenyl­sulfonyl-1H-indol-3-yl)methanone
title_full_unstemmed (Phen­yl)(1-phenyl­sulfonyl-1H-indol-3-yl)methanone
title_short (Phen­yl)(1-phenyl­sulfonyl-1H-indol-3-yl)methanone
title_sort (phen­yl)(1-phenyl­sulfonyl-1h-indol-3-yl)methanone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009149/
https://www.ncbi.nlm.nih.gov/pubmed/21589073
http://dx.doi.org/10.1107/S1600536810042261
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AT dhayalanv phenyl1phenylsulfonyl1hindol3ylmethanone
AT mohanakrishnanak phenyl1phenylsulfonyl1hindol3ylmethanone
AT manivannanv phenyl1phenylsulfonyl1hindol3ylmethanone

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