Ethyl 2-(3,4-dimethoxy­benz­yl)-1-phenyl­sulfonyl-1H-indole-3-carboxyl­ate

In the title compound, C(26)H(25)NO(6)S, the phenyl ring forms a dihedral angle of 82.5 (1)° with the indole ring system. The mol­ecular structure is stabilized by weak intra­molecular C—H⋯O inter­actions and the crystal structure is stabilized by weak inter­molecular C—H⋯O inter­actions....

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Detalles Bibliográficos
Autores principales: Gunasekaran, B., Sureshbabu, Radhakrishnan, 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/PMC2977166/
https://www.ncbi.nlm.nih.gov/pubmed/21583554
http://dx.doi.org/10.1107/S1600536809026506
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author Gunasekaran, B.
Sureshbabu, Radhakrishnan
Mohanakrishnan, A. K.
Chakkaravarthi, G.
Manivannan, V.
author_facet Gunasekaran, B.
Sureshbabu, Radhakrishnan
Mohanakrishnan, A. K.
Chakkaravarthi, G.
Manivannan, V.
author_sort Gunasekaran, B.
collection PubMed
description In the title compound, C(26)H(25)NO(6)S, the phenyl ring forms a dihedral angle of 82.5 (1)° with the indole ring system. The mol­ecular structure is stabilized by weak intra­molecular C—H⋯O inter­actions and the crystal structure is stabilized by weak inter­molecular C—H⋯O inter­actions.
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spelling pubmed-29771662010-12-30 Ethyl 2-(3,4-dimethoxy­benz­yl)-1-phenyl­sulfonyl-1H-indole-3-carboxyl­ate Gunasekaran, B. Sureshbabu, Radhakrishnan Mohanakrishnan, A. K. Chakkaravarthi, G. Manivannan, V. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(26)H(25)NO(6)S, the phenyl ring forms a dihedral angle of 82.5 (1)° with the indole ring system. The mol­ecular structure is stabilized by weak intra­molecular C—H⋯O inter­actions and the crystal structure is stabilized by weak inter­molecular C—H⋯O inter­actions. International Union of Crystallography 2009-07-15 /pmc/articles/PMC2977166/ /pubmed/21583554 http://dx.doi.org/10.1107/S1600536809026506 Text en © Gunasekaran 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
Gunasekaran, B.
Sureshbabu, Radhakrishnan
Mohanakrishnan, A. K.
Chakkaravarthi, G.
Manivannan, V.
Ethyl 2-(3,4-dimethoxy­benz­yl)-1-phenyl­sulfonyl-1H-indole-3-carboxyl­ate
title Ethyl 2-(3,4-dimethoxy­benz­yl)-1-phenyl­sulfonyl-1H-indole-3-carboxyl­ate
title_full Ethyl 2-(3,4-dimethoxy­benz­yl)-1-phenyl­sulfonyl-1H-indole-3-carboxyl­ate
title_fullStr Ethyl 2-(3,4-dimethoxy­benz­yl)-1-phenyl­sulfonyl-1H-indole-3-carboxyl­ate
title_full_unstemmed Ethyl 2-(3,4-dimethoxy­benz­yl)-1-phenyl­sulfonyl-1H-indole-3-carboxyl­ate
title_short Ethyl 2-(3,4-dimethoxy­benz­yl)-1-phenyl­sulfonyl-1H-indole-3-carboxyl­ate
title_sort ethyl 2-(3,4-dimethoxy­benz­yl)-1-phenyl­sulfonyl-1h-indole-3-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977166/
https://www.ncbi.nlm.nih.gov/pubmed/21583554
http://dx.doi.org/10.1107/S1600536809026506
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