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

In the title compound, C(15)H(12)INO(2)S, the sulfonyl-bound phenyl ring forms a dihedral angle 82.84 (9)° with the indole ring system. The mol­ecular structure is stabilized by a weak intra­molecular C—H⋯O hydrogen bond. The crystal structure exhibits weak inter­molecular C—H⋯π inter­actions and π–...

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Detalles Bibliográficos
Autores principales: Ramathilagam, C., Saravanan, Velu, Mohanakrishnan, A. K., Chakkaravarthi, G., Umarani, P. R., Manivannan, V.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051985/
https://www.ncbi.nlm.nih.gov/pubmed/21522386
http://dx.doi.org/10.1107/S1600536811004685
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author Ramathilagam, C.
Saravanan, Velu
Mohanakrishnan, A. K.
Chakkaravarthi, G.
Umarani, P. R.
Manivannan, V.
author_facet Ramathilagam, C.
Saravanan, Velu
Mohanakrishnan, A. K.
Chakkaravarthi, G.
Umarani, P. R.
Manivannan, V.
author_sort Ramathilagam, C.
collection PubMed
description In the title compound, C(15)H(12)INO(2)S, the sulfonyl-bound phenyl ring forms a dihedral angle 82.84 (9)° with the indole ring system. The mol­ecular structure is stabilized by a weak intra­molecular C—H⋯O hydrogen bond. The crystal structure exhibits weak inter­molecular C—H⋯π inter­actions and π–π inter­actions between the indole groups [centroid–centroid distance between the five-membered and six-membered rings of the indole group = 3.7617 (18) Å].
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spelling pubmed-30519852011-04-26 3-Iodo-2-methyl-1-phenyl­sulfonyl-1H-indole Ramathilagam, C. Saravanan, Velu Mohanakrishnan, A. K. Chakkaravarthi, G. Umarani, P. R. Manivannan, V. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(12)INO(2)S, the sulfonyl-bound phenyl ring forms a dihedral angle 82.84 (9)° with the indole ring system. The mol­ecular structure is stabilized by a weak intra­molecular C—H⋯O hydrogen bond. The crystal structure exhibits weak inter­molecular C—H⋯π inter­actions and π–π inter­actions between the indole groups [centroid–centroid distance between the five-membered and six-membered rings of the indole group = 3.7617 (18) Å]. International Union of Crystallography 2011-02-12 /pmc/articles/PMC3051985/ /pubmed/21522386 http://dx.doi.org/10.1107/S1600536811004685 Text en © Ramathilagam et al. 2011 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
Ramathilagam, C.
Saravanan, Velu
Mohanakrishnan, A. K.
Chakkaravarthi, G.
Umarani, P. R.
Manivannan, V.
3-Iodo-2-methyl-1-phenyl­sulfonyl-1H-indole
title 3-Iodo-2-methyl-1-phenyl­sulfonyl-1H-indole
title_full 3-Iodo-2-methyl-1-phenyl­sulfonyl-1H-indole
title_fullStr 3-Iodo-2-methyl-1-phenyl­sulfonyl-1H-indole
title_full_unstemmed 3-Iodo-2-methyl-1-phenyl­sulfonyl-1H-indole
title_short 3-Iodo-2-methyl-1-phenyl­sulfonyl-1H-indole
title_sort 3-iodo-2-methyl-1-phenyl­sulfonyl-1h-indole
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051985/
https://www.ncbi.nlm.nih.gov/pubmed/21522386
http://dx.doi.org/10.1107/S1600536811004685
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AT chakkaravarthig 3iodo2methyl1phenylsulfonyl1hindole
AT umaranipr 3iodo2methyl1phenylsulfonyl1hindole
AT manivannanv 3iodo2methyl1phenylsulfonyl1hindole

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