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3-Bromo­meth­yl-2-chloro­meth­yl-1-phenyl­sulfon­yl-1H-indole

In the title compound, C(16)H(13)BrClNO(2)S, the indole mean plane forms a dihedral angle of 73.59 (19)° with the phenyl ring. The mol­ecular structure is stabilized by weak intra­molecular C—H⋯O inter­actions. The Br atom is disordered over two positions with site occupancy factors of 0.7 and 0.3....

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Detalles Bibliográficos
Autores principales: Chakkaravarthi, G., Dhayalan, V., Mohanakrishnan, A. K., Manivannan, V.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960947/
https://www.ncbi.nlm.nih.gov/pubmed/21202139
http://dx.doi.org/10.1107/S1600536808007678
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author Chakkaravarthi, G.
Dhayalan, V.
Mohanakrishnan, A. K.
Manivannan, V.
author_facet Chakkaravarthi, G.
Dhayalan, V.
Mohanakrishnan, A. K.
Manivannan, V.
author_sort Chakkaravarthi, G.
collection PubMed
description In the title compound, C(16)H(13)BrClNO(2)S, the indole mean plane forms a dihedral angle of 73.59 (19)° with the phenyl ring. The mol­ecular structure is stabilized by weak intra­molecular C—H⋯O inter­actions. The Br atom is disordered over two positions with site occupancy factors of 0.7 and 0.3.
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spelling pubmed-29609472010-12-30 3-Bromo­meth­yl-2-chloro­meth­yl-1-phenyl­sulfon­yl-1H-indole Chakkaravarthi, G. Dhayalan, V. Mohanakrishnan, A. K. Manivannan, V. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(13)BrClNO(2)S, the indole mean plane forms a dihedral angle of 73.59 (19)° with the phenyl ring. The mol­ecular structure is stabilized by weak intra­molecular C—H⋯O inter­actions. The Br atom is disordered over two positions with site occupancy factors of 0.7 and 0.3. International Union of Crystallography 2008-03-29 /pmc/articles/PMC2960947/ /pubmed/21202139 http://dx.doi.org/10.1107/S1600536808007678 Text en © Chakkaravarthi 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
Chakkaravarthi, G.
Dhayalan, V.
Mohanakrishnan, A. K.
Manivannan, V.
3-Bromo­meth­yl-2-chloro­meth­yl-1-phenyl­sulfon­yl-1H-indole
title 3-Bromo­meth­yl-2-chloro­meth­yl-1-phenyl­sulfon­yl-1H-indole
title_full 3-Bromo­meth­yl-2-chloro­meth­yl-1-phenyl­sulfon­yl-1H-indole
title_fullStr 3-Bromo­meth­yl-2-chloro­meth­yl-1-phenyl­sulfon­yl-1H-indole
title_full_unstemmed 3-Bromo­meth­yl-2-chloro­meth­yl-1-phenyl­sulfon­yl-1H-indole
title_short 3-Bromo­meth­yl-2-chloro­meth­yl-1-phenyl­sulfon­yl-1H-indole
title_sort 3-bromo­meth­yl-2-chloro­meth­yl-1-phenyl­sulfon­yl-1h-indole
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960947/
https://www.ncbi.nlm.nih.gov/pubmed/21202139
http://dx.doi.org/10.1107/S1600536808007678
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