3-Benzoyl-4-hydr­oxy-2-methyl-2H-1,2-benzothia­zine 1,1-dioxide

In the title mol­ecule, C(16)H(13)NO(4)S, the heterocyclic thia­zine ring adopts a half-chair conformation with the S and N atoms displaced by 0.410 (3) and 0.299 (3) Å, respectively, on opposite sides of the mean plane formed by the remaining ring atoms. The crystal structure is stabilized by inter...

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Detalles Bibliográficos
Autores principales: Ahmad, Matloob, Siddiqui, Hamid Latif, Ahmad, Saeed, Aslam, Sana, Parvez, Masood
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983979/
https://www.ncbi.nlm.nih.gov/pubmed/21580768
http://dx.doi.org/10.1107/S1600536810011025
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author Ahmad, Matloob
Siddiqui, Hamid Latif
Ahmad, Saeed
Aslam, Sana
Parvez, Masood
author_facet Ahmad, Matloob
Siddiqui, Hamid Latif
Ahmad, Saeed
Aslam, Sana
Parvez, Masood
author_sort Ahmad, Matloob
collection PubMed
description In the title mol­ecule, C(16)H(13)NO(4)S, the heterocyclic thia­zine ring adopts a half-chair conformation with the S and N atoms displaced by 0.410 (3) and 0.299 (3) Å, respectively, on opposite sides of the mean plane formed by the remaining ring atoms. The crystal structure is stabilized by inter­molecular hydrogen bonds of the types O—H⋯O and C—H⋯O; the former result in dimers lying about inversion centers and the latter form chains of mol­ecules running along the c axis. In addition, intra­molecular O—H⋯O links are present.
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spelling pubmed-29839792010-12-30 3-Benzoyl-4-hydr­oxy-2-methyl-2H-1,2-benzothia­zine 1,1-dioxide Ahmad, Matloob Siddiqui, Hamid Latif Ahmad, Saeed Aslam, Sana Parvez, Masood Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title mol­ecule, C(16)H(13)NO(4)S, the heterocyclic thia­zine ring adopts a half-chair conformation with the S and N atoms displaced by 0.410 (3) and 0.299 (3) Å, respectively, on opposite sides of the mean plane formed by the remaining ring atoms. The crystal structure is stabilized by inter­molecular hydrogen bonds of the types O—H⋯O and C—H⋯O; the former result in dimers lying about inversion centers and the latter form chains of mol­ecules running along the c axis. In addition, intra­molecular O—H⋯O links are present. International Union of Crystallography 2010-03-27 /pmc/articles/PMC2983979/ /pubmed/21580768 http://dx.doi.org/10.1107/S1600536810011025 Text en © Ahmad 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
Ahmad, Matloob
Siddiqui, Hamid Latif
Ahmad, Saeed
Aslam, Sana
Parvez, Masood
3-Benzoyl-4-hydr­oxy-2-methyl-2H-1,2-benzothia­zine 1,1-dioxide
title 3-Benzoyl-4-hydr­oxy-2-methyl-2H-1,2-benzothia­zine 1,1-dioxide
title_full 3-Benzoyl-4-hydr­oxy-2-methyl-2H-1,2-benzothia­zine 1,1-dioxide
title_fullStr 3-Benzoyl-4-hydr­oxy-2-methyl-2H-1,2-benzothia­zine 1,1-dioxide
title_full_unstemmed 3-Benzoyl-4-hydr­oxy-2-methyl-2H-1,2-benzothia­zine 1,1-dioxide
title_short 3-Benzoyl-4-hydr­oxy-2-methyl-2H-1,2-benzothia­zine 1,1-dioxide
title_sort 3-benzoyl-4-hydr­oxy-2-methyl-2h-1,2-benzothia­zine 1,1-dioxide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983979/
https://www.ncbi.nlm.nih.gov/pubmed/21580768
http://dx.doi.org/10.1107/S1600536810011025
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