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N-(2-Formylphenyl)benzenesulfonamide
In the title compound, C(13)H(11)NO(3)S, the two aromatic rings are oriented at an angle of 88.18 (8)°. Intramolecular N—H⋯O and C—H⋯O hydrogen bonds are observed, each of which generates an S(6) ring motif. In the crystal, molecules are linked into C(7) chains along [010] by intermolecular C—H⋯O...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969910/ https://www.ncbi.nlm.nih.gov/pubmed/21577611 http://dx.doi.org/10.1107/S1600536809032681 |
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author | Thenmozhi, S. Ranjith, S. SubbiahPandi, A. Dhayalan, V. MohanaKrishnan, A. K. |
author_facet | Thenmozhi, S. Ranjith, S. SubbiahPandi, A. Dhayalan, V. MohanaKrishnan, A. K. |
author_sort | Thenmozhi, S. |
collection | PubMed |
description | In the title compound, C(13)H(11)NO(3)S, the two aromatic rings are oriented at an angle of 88.18 (8)°. Intramolecular N—H⋯O and C—H⋯O hydrogen bonds are observed, each of which generates an S(6) ring motif. In the crystal, molecules are linked into C(7) chains along [010] by intermolecular C—H⋯O hydrogen bonds. The structure is further stabilized by intermolecular C—H⋯π interactions involving the sulfonyl-bound phenyl ring. |
format | Text |
id | pubmed-2969910 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29699102010-12-30 N-(2-Formylphenyl)benzenesulfonamide Thenmozhi, S. Ranjith, S. SubbiahPandi, A. Dhayalan, V. MohanaKrishnan, A. K. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(11)NO(3)S, the two aromatic rings are oriented at an angle of 88.18 (8)°. Intramolecular N—H⋯O and C—H⋯O hydrogen bonds are observed, each of which generates an S(6) ring motif. In the crystal, molecules are linked into C(7) chains along [010] by intermolecular C—H⋯O hydrogen bonds. The structure is further stabilized by intermolecular C—H⋯π interactions involving the sulfonyl-bound phenyl ring. International Union of Crystallography 2009-08-22 /pmc/articles/PMC2969910/ /pubmed/21577611 http://dx.doi.org/10.1107/S1600536809032681 Text en © Thenmozhi 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 Thenmozhi, S. Ranjith, S. SubbiahPandi, A. Dhayalan, V. MohanaKrishnan, A. K. N-(2-Formylphenyl)benzenesulfonamide |
title |
N-(2-Formylphenyl)benzenesulfonamide |
title_full |
N-(2-Formylphenyl)benzenesulfonamide |
title_fullStr |
N-(2-Formylphenyl)benzenesulfonamide |
title_full_unstemmed |
N-(2-Formylphenyl)benzenesulfonamide |
title_short |
N-(2-Formylphenyl)benzenesulfonamide |
title_sort | n-(2-formylphenyl)benzenesulfonamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969910/ https://www.ncbi.nlm.nih.gov/pubmed/21577611 http://dx.doi.org/10.1107/S1600536809032681 |
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