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Ethyl 2-[N-(2-formylphenyl)benzenesulfonamido]acetate
In the molecule of the title compound, C(17)H(17)NO(5)S, the two aromatic rings are oriented at an angle of 30.13 (10)°. The ethyl acetate group assumes an extended conformation. Molecules are linked into C(7) chains running along the a axis by intermolecular C—H⋯O hydrogen bonds, and the chains...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968473/ https://www.ncbi.nlm.nih.gov/pubmed/21582152 http://dx.doi.org/10.1107/S160053680900292X |
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author | Ranjith, S. Sugumar, P. Sureshbabu, R. Mohanakrishnan, A. K. Ponnuswamy, M. N. |
author_facet | Ranjith, S. Sugumar, P. Sureshbabu, R. Mohanakrishnan, A. K. Ponnuswamy, M. N. |
author_sort | Ranjith, S. |
collection | PubMed |
description | In the molecule of the title compound, C(17)H(17)NO(5)S, the two aromatic rings are oriented at an angle of 30.13 (10)°. The ethyl acetate group assumes an extended conformation. Molecules are linked into C(7) chains running along the a axis by intermolecular C—H⋯O hydrogen bonds, and the chains are crosslinked via C—H⋯π interactions, with the sulfonyl-bound phenyl ring acting as an acceptor. |
format | Text |
id | pubmed-2968473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29684732010-12-30 Ethyl 2-[N-(2-formylphenyl)benzenesulfonamido]acetate Ranjith, S. Sugumar, P. Sureshbabu, R. Mohanakrishnan, A. K. Ponnuswamy, M. N. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the molecule of the title compound, C(17)H(17)NO(5)S, the two aromatic rings are oriented at an angle of 30.13 (10)°. The ethyl acetate group assumes an extended conformation. Molecules are linked into C(7) chains running along the a axis by intermolecular C—H⋯O hydrogen bonds, and the chains are crosslinked via C—H⋯π interactions, with the sulfonyl-bound phenyl ring acting as an acceptor. International Union of Crystallography 2009-02-06 /pmc/articles/PMC2968473/ /pubmed/21582152 http://dx.doi.org/10.1107/S160053680900292X Text en © Ranjith 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 Ranjith, S. Sugumar, P. Sureshbabu, R. Mohanakrishnan, A. K. Ponnuswamy, M. N. Ethyl 2-[N-(2-formylphenyl)benzenesulfonamido]acetate |
title | Ethyl 2-[N-(2-formylphenyl)benzenesulfonamido]acetate |
title_full | Ethyl 2-[N-(2-formylphenyl)benzenesulfonamido]acetate |
title_fullStr | Ethyl 2-[N-(2-formylphenyl)benzenesulfonamido]acetate |
title_full_unstemmed | Ethyl 2-[N-(2-formylphenyl)benzenesulfonamido]acetate |
title_short | Ethyl 2-[N-(2-formylphenyl)benzenesulfonamido]acetate |
title_sort | ethyl 2-[n-(2-formylphenyl)benzenesulfonamido]acetate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968473/ https://www.ncbi.nlm.nih.gov/pubmed/21582152 http://dx.doi.org/10.1107/S160053680900292X |
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