Ethyl 2-[(phenyl­sulfan­yl)meth­yl]-1-(phenyl­sulfon­yl)-1H-indole-3-carboxyl­ate

In the title compound, C(24)H(21)NO(4)S(2), the phenyl rings form dihedral angles of 85.77 (9) and 85.22 (9)° and the ester group forms an angle of 12.61 (10)° with the indane ring. The mol­ecular structure is stabilized by weak intra­molecular C—H⋯O inter­actions.

Detalles Bibliográficos
Autores principales: Chakkaravarthi, G., Dhayalan, V., Mohanakrishnan, A. K., Manivannan, V.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960260/
https://www.ncbi.nlm.nih.gov/pubmed/21201422
http://dx.doi.org/10.1107/S1600536807068778
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author Chakkaravarthi, G.
Dhayalan, V.
Mohanakrishnan, A. K.
Manivannan, V.
author_facet Chakkaravarthi, G.
Dhayalan, V.
Mohanakrishnan, A. K.
Manivannan, V.
author_sort Chakkaravarthi, G.
collection PubMed
description In the title compound, C(24)H(21)NO(4)S(2), the phenyl rings form dihedral angles of 85.77 (9) and 85.22 (9)° and the ester group forms an angle of 12.61 (10)° with the indane ring. The mol­ecular structure is stabilized by weak intra­molecular C—H⋯O inter­actions.
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spelling pubmed-29602602010-12-30 Ethyl 2-[(phenyl­sulfan­yl)meth­yl]-1-(phenyl­sulfon­yl)-1H-indole-3-carboxyl­ate Chakkaravarthi, G. Dhayalan, V. Mohanakrishnan, A. K. Manivannan, V. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(24)H(21)NO(4)S(2), the phenyl rings form dihedral angles of 85.77 (9) and 85.22 (9)° and the ester group forms an angle of 12.61 (10)° with the indane ring. The mol­ecular structure is stabilized by weak intra­molecular C—H⋯O inter­actions. International Union of Crystallography 2008-01-09 /pmc/articles/PMC2960260/ /pubmed/21201422 http://dx.doi.org/10.1107/S1600536807068778 Text en © Chakkaravarthi et al. 2008 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
Chakkaravarthi, G.
Dhayalan, V.
Mohanakrishnan, A. K.
Manivannan, V.
Ethyl 2-[(phenyl­sulfan­yl)meth­yl]-1-(phenyl­sulfon­yl)-1H-indole-3-carboxyl­ate
title Ethyl 2-[(phenyl­sulfan­yl)meth­yl]-1-(phenyl­sulfon­yl)-1H-indole-3-carboxyl­ate
title_full Ethyl 2-[(phenyl­sulfan­yl)meth­yl]-1-(phenyl­sulfon­yl)-1H-indole-3-carboxyl­ate
title_fullStr Ethyl 2-[(phenyl­sulfan­yl)meth­yl]-1-(phenyl­sulfon­yl)-1H-indole-3-carboxyl­ate
title_full_unstemmed Ethyl 2-[(phenyl­sulfan­yl)meth­yl]-1-(phenyl­sulfon­yl)-1H-indole-3-carboxyl­ate
title_short Ethyl 2-[(phenyl­sulfan­yl)meth­yl]-1-(phenyl­sulfon­yl)-1H-indole-3-carboxyl­ate
title_sort ethyl 2-[(phenyl­sulfan­yl)meth­yl]-1-(phenyl­sulfon­yl)-1h-indole-3-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960260/
https://www.ncbi.nlm.nih.gov/pubmed/21201422
http://dx.doi.org/10.1107/S1600536807068778
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AT mohanakrishnanak ethyl2phenylsulfanylmethyl1phenylsulfonyl1hindole3carboxylate
AT manivannanv ethyl2phenylsulfanylmethyl1phenylsulfonyl1hindole3carboxylate

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