2-Chloro­methyl-3-methyl-1-phenyl­sulfonyl-1H-indole

In the title compound, C(16)H(14)ClNO(2)S, the phenyl ring makes a dihedral angle of 78.1 (1)° with the indole ring system. The mol­ecular structure is stabilized by weak intra­molecular C—H⋯O inter­actions. The crystal structure exhibits weak inter­molecular C—H⋯O, C—H⋯π and π–π [centroid–centroid...

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Detalles Bibliográficos
Autores principales: Saravanan, B., Dhayalan, V., Mohanakrishnan, A. K., Chakkaravarthi, G., Manivannan, V.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970994/
https://www.ncbi.nlm.nih.gov/pubmed/21578328
http://dx.doi.org/10.1107/S1600536809041191
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author Saravanan, B.
Dhayalan, V.
Mohanakrishnan, A. K.
Chakkaravarthi, G.
Manivannan, V.
author_facet Saravanan, B.
Dhayalan, V.
Mohanakrishnan, A. K.
Chakkaravarthi, G.
Manivannan, V.
author_sort Saravanan, B.
collection PubMed
description In the title compound, C(16)H(14)ClNO(2)S, the phenyl ring makes a dihedral angle of 78.1 (1)° with the indole ring system. The mol­ecular structure is stabilized by weak intra­molecular C—H⋯O inter­actions. The crystal structure exhibits weak inter­molecular C—H⋯O, C—H⋯π and π–π [centroid–centroid distances = 3.620 (1)–3.794 (1) Å] inter­actions.
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spelling pubmed-29709942010-12-30 2-Chloro­methyl-3-methyl-1-phenyl­sulfonyl-1H-indole Saravanan, B. Dhayalan, V. Mohanakrishnan, A. K. Chakkaravarthi, G. Manivannan, V. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(14)ClNO(2)S, the phenyl ring makes a dihedral angle of 78.1 (1)° with the indole ring system. The mol­ecular structure is stabilized by weak intra­molecular C—H⋯O inter­actions. The crystal structure exhibits weak inter­molecular C—H⋯O, C—H⋯π and π–π [centroid–centroid distances = 3.620 (1)–3.794 (1) Å] inter­actions. International Union of Crystallography 2009-10-17 /pmc/articles/PMC2970994/ /pubmed/21578328 http://dx.doi.org/10.1107/S1600536809041191 Text en © Saravanan et al. 2009 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
Saravanan, B.
Dhayalan, V.
Mohanakrishnan, A. K.
Chakkaravarthi, G.
Manivannan, V.
2-Chloro­methyl-3-methyl-1-phenyl­sulfonyl-1H-indole
title 2-Chloro­methyl-3-methyl-1-phenyl­sulfonyl-1H-indole
title_full 2-Chloro­methyl-3-methyl-1-phenyl­sulfonyl-1H-indole
title_fullStr 2-Chloro­methyl-3-methyl-1-phenyl­sulfonyl-1H-indole
title_full_unstemmed 2-Chloro­methyl-3-methyl-1-phenyl­sulfonyl-1H-indole
title_short 2-Chloro­methyl-3-methyl-1-phenyl­sulfonyl-1H-indole
title_sort 2-chloro­methyl-3-methyl-1-phenyl­sulfonyl-1h-indole
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970994/
https://www.ncbi.nlm.nih.gov/pubmed/21578328
http://dx.doi.org/10.1107/S1600536809041191
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AT mohanakrishnanak 2chloromethyl3methyl1phenylsulfonyl1hindole
AT chakkaravarthig 2chloromethyl3methyl1phenylsulfonyl1hindole
AT manivannanv 2chloromethyl3methyl1phenylsulfonyl1hindole

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