2-Methyl-1-phenyl­sulfonyl-1H-indole-3-carbaldehyde

In the title compound, C(16)H(13)NO(3)S, the sulfonyl-bound phenyl ring forms a dihedral angle of 84.17 (6)° with the indole ring system. An intra­molecular C—H⋯O hydrogen bond generates an S(6) ring motif. The crystal structure exhibits weak inter­molecular C—H⋯O hydrogen bonds and π–π inter­action...

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Autores principales: Ramathilagam, C., Saravanan, V., Mohanakrishnan, A. K., Umarani, P. R., Manivannan, V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201221/
https://www.ncbi.nlm.nih.gov/pubmed/22058759
http://dx.doi.org/10.1107/S1600536811035665
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author Ramathilagam, C.
Saravanan, V.
Mohanakrishnan, A. K.
Umarani, P. R.
Manivannan, V.
author_facet Ramathilagam, C.
Saravanan, V.
Mohanakrishnan, A. K.
Umarani, P. R.
Manivannan, V.
author_sort Ramathilagam, C.
collection PubMed
description In the title compound, C(16)H(13)NO(3)S, the sulfonyl-bound phenyl ring forms a dihedral angle of 84.17 (6)° with the indole ring system. An intra­molecular C—H⋯O hydrogen bond generates an S(6) ring motif. The crystal structure exhibits weak inter­molecular C—H⋯O hydrogen bonds and π–π inter­actions between the five- and six-membered rings of the indole group [centroid–centroid distance = 3.6871 (9) Å].
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spelling pubmed-32012212011-11-06 2-Methyl-1-phenyl­sulfonyl-1H-indole-3-carbaldehyde Ramathilagam, C. Saravanan, V. Mohanakrishnan, A. K. Umarani, P. R. Manivannan, V. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(13)NO(3)S, the sulfonyl-bound phenyl ring forms a dihedral angle of 84.17 (6)° with the indole ring system. An intra­molecular C—H⋯O hydrogen bond generates an S(6) ring motif. The crystal structure exhibits weak inter­molecular C—H⋯O hydrogen bonds and π–π inter­actions between the five- and six-membered rings of the indole group [centroid–centroid distance = 3.6871 (9) Å]. International Union of Crystallography 2011-09-14 /pmc/articles/PMC3201221/ /pubmed/22058759 http://dx.doi.org/10.1107/S1600536811035665 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, V.
Mohanakrishnan, A. K.
Umarani, P. R.
Manivannan, V.
2-Methyl-1-phenyl­sulfonyl-1H-indole-3-carbaldehyde
title 2-Methyl-1-phenyl­sulfonyl-1H-indole-3-carbaldehyde
title_full 2-Methyl-1-phenyl­sulfonyl-1H-indole-3-carbaldehyde
title_fullStr 2-Methyl-1-phenyl­sulfonyl-1H-indole-3-carbaldehyde
title_full_unstemmed 2-Methyl-1-phenyl­sulfonyl-1H-indole-3-carbaldehyde
title_short 2-Methyl-1-phenyl­sulfonyl-1H-indole-3-carbaldehyde
title_sort 2-methyl-1-phenyl­sulfonyl-1h-indole-3-carbaldehyde
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201221/
https://www.ncbi.nlm.nih.gov/pubmed/22058759
http://dx.doi.org/10.1107/S1600536811035665
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AT mohanakrishnanak 2methyl1phenylsulfonyl1hindole3carbaldehyde
AT umaranipr 2methyl1phenylsulfonyl1hindole3carbaldehyde
AT manivannanv 2methyl1phenylsulfonyl1hindole3carbaldehyde

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