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3-(3-Chlorobenzoyl)-4-hydroxy-2H-1,2-benzothiazine 1,1-dioxide
In the title compound, C(15)H(10)ClNO(4)S, the heterocyclic thiazine ring adopts a half-chair conformation with the S and N atoms displaced by 0.476 (5) and 0.227 (5) Å, respectively, on opposite sides of the mean plane formed by the remaining ring atoms. The structure is stabilized by intermolecu...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2984067/ https://www.ncbi.nlm.nih.gov/pubmed/21580703 http://dx.doi.org/10.1107/S1600536810009761 |
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author | Khalid, Zunera Siddiqui, Hamid Latif Ahmad, Matloob Aslam, Sana Parvez, Masood |
author_facet | Khalid, Zunera Siddiqui, Hamid Latif Ahmad, Matloob Aslam, Sana Parvez, Masood |
author_sort | Khalid, Zunera |
collection | PubMed |
description | In the title compound, C(15)H(10)ClNO(4)S, the heterocyclic thiazine ring adopts a half-chair conformation with the S and N atoms displaced by 0.476 (5) and 0.227 (5) Å, respectively, on opposite sides of the mean plane formed by the remaining ring atoms. The structure is stabilized by intermolecular N—H⋯O and C—H⋯O hydrogen bonds. In addition, intramolecular O—H⋯O and C—H⋯N interactions are also present. |
format | Text |
id | pubmed-2984067 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29840672010-12-30 3-(3-Chlorobenzoyl)-4-hydroxy-2H-1,2-benzothiazine 1,1-dioxide Khalid, Zunera Siddiqui, Hamid Latif Ahmad, Matloob Aslam, Sana Parvez, Masood Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(10)ClNO(4)S, the heterocyclic thiazine ring adopts a half-chair conformation with the S and N atoms displaced by 0.476 (5) and 0.227 (5) Å, respectively, on opposite sides of the mean plane formed by the remaining ring atoms. The structure is stabilized by intermolecular N—H⋯O and C—H⋯O hydrogen bonds. In addition, intramolecular O—H⋯O and C—H⋯N interactions are also present. International Union of Crystallography 2010-03-20 /pmc/articles/PMC2984067/ /pubmed/21580703 http://dx.doi.org/10.1107/S1600536810009761 Text en © Khalid et al. 2010 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 Khalid, Zunera Siddiqui, Hamid Latif Ahmad, Matloob Aslam, Sana Parvez, Masood 3-(3-Chlorobenzoyl)-4-hydroxy-2H-1,2-benzothiazine 1,1-dioxide |
title | 3-(3-Chlorobenzoyl)-4-hydroxy-2H-1,2-benzothiazine 1,1-dioxide |
title_full | 3-(3-Chlorobenzoyl)-4-hydroxy-2H-1,2-benzothiazine 1,1-dioxide |
title_fullStr | 3-(3-Chlorobenzoyl)-4-hydroxy-2H-1,2-benzothiazine 1,1-dioxide |
title_full_unstemmed | 3-(3-Chlorobenzoyl)-4-hydroxy-2H-1,2-benzothiazine 1,1-dioxide |
title_short | 3-(3-Chlorobenzoyl)-4-hydroxy-2H-1,2-benzothiazine 1,1-dioxide |
title_sort | 3-(3-chlorobenzoyl)-4-hydroxy-2h-1,2-benzothiazine 1,1-dioxide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2984067/ https://www.ncbi.nlm.nih.gov/pubmed/21580703 http://dx.doi.org/10.1107/S1600536810009761 |
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