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(E)-3-Phenyl-2-(1-tosyl-1H-indol-3-ylcarbonyl)acrylonitrile
In the title compound, C(25)H(18)N(2)O(3)S, the indole moiety is planar and makes a dihedral angle of 89.95 (09)° with the phenyl ring of the sulfonyl substituent. The molecular conformation features a weak C—H⋯N short contact and the crystal packing reveals a weak C—H⋯O hydrogen bond.
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295467/ https://www.ncbi.nlm.nih.gov/pubmed/22412578 http://dx.doi.org/10.1107/S1600536812004886 |
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author | Paramasivam, S. Bhaskar, G. Seshadri, P. R. Perumal, P. T. |
author_facet | Paramasivam, S. Bhaskar, G. Seshadri, P. R. Perumal, P. T. |
author_sort | Paramasivam, S. |
collection | PubMed |
description | In the title compound, C(25)H(18)N(2)O(3)S, the indole moiety is planar and makes a dihedral angle of 89.95 (09)° with the phenyl ring of the sulfonyl substituent. The molecular conformation features a weak C—H⋯N short contact and the crystal packing reveals a weak C—H⋯O hydrogen bond. |
format | Online Article Text |
id | pubmed-3295467 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32954672012-03-12 (E)-3-Phenyl-2-(1-tosyl-1H-indol-3-ylcarbonyl)acrylonitrile Paramasivam, S. Bhaskar, G. Seshadri, P. R. Perumal, P. T. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(25)H(18)N(2)O(3)S, the indole moiety is planar and makes a dihedral angle of 89.95 (09)° with the phenyl ring of the sulfonyl substituent. The molecular conformation features a weak C—H⋯N short contact and the crystal packing reveals a weak C—H⋯O hydrogen bond. International Union of Crystallography 2012-02-10 /pmc/articles/PMC3295467/ /pubmed/22412578 http://dx.doi.org/10.1107/S1600536812004886 Text en © Paramasivam et al. 2012 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 Paramasivam, S. Bhaskar, G. Seshadri, P. R. Perumal, P. T. (E)-3-Phenyl-2-(1-tosyl-1H-indol-3-ylcarbonyl)acrylonitrile |
title | (E)-3-Phenyl-2-(1-tosyl-1H-indol-3-ylcarbonyl)acrylonitrile |
title_full | (E)-3-Phenyl-2-(1-tosyl-1H-indol-3-ylcarbonyl)acrylonitrile |
title_fullStr | (E)-3-Phenyl-2-(1-tosyl-1H-indol-3-ylcarbonyl)acrylonitrile |
title_full_unstemmed | (E)-3-Phenyl-2-(1-tosyl-1H-indol-3-ylcarbonyl)acrylonitrile |
title_short | (E)-3-Phenyl-2-(1-tosyl-1H-indol-3-ylcarbonyl)acrylonitrile |
title_sort | (e)-3-phenyl-2-(1-tosyl-1h-indol-3-ylcarbonyl)acrylonitrile |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295467/ https://www.ncbi.nlm.nih.gov/pubmed/22412578 http://dx.doi.org/10.1107/S1600536812004886 |
work_keys_str_mv | AT paramasivams e3phenyl21tosyl1hindol3ylcarbonylacrylonitrile AT bhaskarg e3phenyl21tosyl1hindol3ylcarbonylacrylonitrile AT seshadripr e3phenyl21tosyl1hindol3ylcarbonylacrylonitrile AT perumalpt e3phenyl21tosyl1hindol3ylcarbonylacrylonitrile |