(Z)-3-(1-Chloro­prop-1-en­yl)-2-methyl-1-phenyl­sulfonyl-1H-indole

In the title compound, C(18)H(16)ClNO(2)S, the indole ring system forms a dihedral angle of 75.07 (8)° with the phenyl ring. The mol­ecular structure is stabilized by a weak intra­molecular C—H⋯O hydrogen bond. In the crystal, mol­ecules are linked by weak C—H⋯O hydrogen bonds, forming a chain along...

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Detalles Bibliográficos
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:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885050/
https://www.ncbi.nlm.nih.gov/pubmed/24454226
http://dx.doi.org/10.1107/S1600536813030730
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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(18)H(16)ClNO(2)S, the indole ring system forms a dihedral angle of 75.07 (8)° with the phenyl ring. The mol­ecular structure is stabilized by a weak intra­molecular C—H⋯O hydrogen bond. In the crystal, mol­ecules are linked by weak C—H⋯O hydrogen bonds, forming a chain along [10-1]. C—H⋯π inter­actions are also observed, leading to a three-dimensional network.
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spelling pubmed-38850502014-01-17 (Z)-3-(1-Chloro­prop-1-en­yl)-2-methyl-1-phenyl­sulfonyl-1H-indole 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(18)H(16)ClNO(2)S, the indole ring system forms a dihedral angle of 75.07 (8)° with the phenyl ring. The mol­ecular structure is stabilized by a weak intra­molecular C—H⋯O hydrogen bond. In the crystal, mol­ecules are linked by weak C—H⋯O hydrogen bonds, forming a chain along [10-1]. C—H⋯π inter­actions are also observed, leading to a three-dimensional network. International Union of Crystallography 2013-11-16 /pmc/articles/PMC3885050/ /pubmed/24454226 http://dx.doi.org/10.1107/S1600536813030730 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.
(Z)-3-(1-Chloro­prop-1-en­yl)-2-methyl-1-phenyl­sulfonyl-1H-indole
title (Z)-3-(1-Chloro­prop-1-en­yl)-2-methyl-1-phenyl­sulfonyl-1H-indole
title_full (Z)-3-(1-Chloro­prop-1-en­yl)-2-methyl-1-phenyl­sulfonyl-1H-indole
title_fullStr (Z)-3-(1-Chloro­prop-1-en­yl)-2-methyl-1-phenyl­sulfonyl-1H-indole
title_full_unstemmed (Z)-3-(1-Chloro­prop-1-en­yl)-2-methyl-1-phenyl­sulfonyl-1H-indole
title_short (Z)-3-(1-Chloro­prop-1-en­yl)-2-methyl-1-phenyl­sulfonyl-1H-indole
title_sort (z)-3-(1-chloro­prop-1-en­yl)-2-methyl-1-phenyl­sulfonyl-1h-indole
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885050/
https://www.ncbi.nlm.nih.gov/pubmed/24454226
http://dx.doi.org/10.1107/S1600536813030730
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