(4-Bromo­phen­yl)(1-phenyl­sulfonyl-1H-indol-2-yl)methanone

In the title compound, C(21)H(14)BrNO(3)S, the indole ring system forms dihedral angles of 65.64 (8) and 59.30 (8)°, respectively, with the phenyl and bromo­phenyl rings. In the crystal, mol­ecules are connected by a C—H⋯O hydrogen bond, forming a chain along [101]. The chains are further connected...

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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/PMC3009294/
https://www.ncbi.nlm.nih.gov/pubmed/21589125
http://dx.doi.org/10.1107/S160053681004198X
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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(14)BrNO(3)S, the indole ring system forms dihedral angles of 65.64 (8) and 59.30 (8)°, respectively, with the phenyl and bromo­phenyl rings. In the crystal, mol­ecules are connected by a C—H⋯O hydrogen bond, forming a chain along [101]. The chains are further connected by weak inter­molecular C—H⋯π inter­actions, forming a layer parallel to the ac plane.
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spelling pubmed-30092942010-12-30 (4-Bromo­phen­yl)(1-phenyl­sulfonyl-1H-indol-2-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(14)BrNO(3)S, the indole ring system forms dihedral angles of 65.64 (8) and 59.30 (8)°, respectively, with the phenyl and bromo­phenyl rings. In the crystal, mol­ecules are connected by a C—H⋯O hydrogen bond, forming a chain along [101]. The chains are further connected by weak inter­molecular C—H⋯π inter­actions, forming a layer parallel to the ac plane. International Union of Crystallography 2010-10-30 /pmc/articles/PMC3009294/ /pubmed/21589125 http://dx.doi.org/10.1107/S160053681004198X 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.
(4-Bromo­phen­yl)(1-phenyl­sulfonyl-1H-indol-2-yl)methanone
title (4-Bromo­phen­yl)(1-phenyl­sulfonyl-1H-indol-2-yl)methanone
title_full (4-Bromo­phen­yl)(1-phenyl­sulfonyl-1H-indol-2-yl)methanone
title_fullStr (4-Bromo­phen­yl)(1-phenyl­sulfonyl-1H-indol-2-yl)methanone
title_full_unstemmed (4-Bromo­phen­yl)(1-phenyl­sulfonyl-1H-indol-2-yl)methanone
title_short (4-Bromo­phen­yl)(1-phenyl­sulfonyl-1H-indol-2-yl)methanone
title_sort (4-bromo­phen­yl)(1-phenyl­sulfonyl-1h-indol-2-yl)methanone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009294/
https://www.ncbi.nlm.nih.gov/pubmed/21589125
http://dx.doi.org/10.1107/S160053681004198X
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