Methyl 4-eth­oxy-2-methyl-2H-1,2-benzothia­zine-3-carboxyl­ate 1,1-dioxide

In the crystal structure of the title compound, C(13)H(15)NO(5)S, the mol­ecules exhibit weak S=O⋯H—C and C=O⋯H—C inter­molecular inter­actions and arrange themselves into centrosymmetric dimers by means of π–π inter­actions (ring centroids are separated by 3.619 Å, while the closest C⋯C contacts ar...

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Autores principales: Zia-ur-Rehman, Muhammad, Choudary, Jamil Anwar, Elsegood, Mark R. J., Akbar, Noshin, Latif Siddiqui, Hamid
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962229/
https://www.ncbi.nlm.nih.gov/pubmed/21203217
http://dx.doi.org/10.1107/S1600536808021363
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author Zia-ur-Rehman, Muhammad
Choudary, Jamil Anwar
Elsegood, Mark R. J.
Akbar, Noshin
Latif Siddiqui, Hamid
author_facet Zia-ur-Rehman, Muhammad
Choudary, Jamil Anwar
Elsegood, Mark R. J.
Akbar, Noshin
Latif Siddiqui, Hamid
author_sort Zia-ur-Rehman, Muhammad
collection PubMed
description In the crystal structure of the title compound, C(13)H(15)NO(5)S, the mol­ecules exhibit weak S=O⋯H—C and C=O⋯H—C inter­molecular inter­actions and arrange themselves into centrosymmetric dimers by means of π–π inter­actions (ring centroids are separated by 3.619 Å, while the closest C⋯C contacts are 3.514 Å). 1,2-Benzothia­zines of this kind have a range of biological activities and are used as medicines in the treatment of inflammation and rheumatoid arthritis.
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spelling pubmed-29622292010-12-30 Methyl 4-eth­oxy-2-methyl-2H-1,2-benzothia­zine-3-carboxyl­ate 1,1-dioxide Zia-ur-Rehman, Muhammad Choudary, Jamil Anwar Elsegood, Mark R. J. Akbar, Noshin Latif Siddiqui, Hamid Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(13)H(15)NO(5)S, the mol­ecules exhibit weak S=O⋯H—C and C=O⋯H—C inter­molecular inter­actions and arrange themselves into centrosymmetric dimers by means of π–π inter­actions (ring centroids are separated by 3.619 Å, while the closest C⋯C contacts are 3.514 Å). 1,2-Benzothia­zines of this kind have a range of biological activities and are used as medicines in the treatment of inflammation and rheumatoid arthritis. International Union of Crystallography 2008-07-16 /pmc/articles/PMC2962229/ /pubmed/21203217 http://dx.doi.org/10.1107/S1600536808021363 Text en © Zia-ur-Rehman et al. 2008 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
Zia-ur-Rehman, Muhammad
Choudary, Jamil Anwar
Elsegood, Mark R. J.
Akbar, Noshin
Latif Siddiqui, Hamid
Methyl 4-eth­oxy-2-methyl-2H-1,2-benzothia­zine-3-carboxyl­ate 1,1-dioxide
title Methyl 4-eth­oxy-2-methyl-2H-1,2-benzothia­zine-3-carboxyl­ate 1,1-dioxide
title_full Methyl 4-eth­oxy-2-methyl-2H-1,2-benzothia­zine-3-carboxyl­ate 1,1-dioxide
title_fullStr Methyl 4-eth­oxy-2-methyl-2H-1,2-benzothia­zine-3-carboxyl­ate 1,1-dioxide
title_full_unstemmed Methyl 4-eth­oxy-2-methyl-2H-1,2-benzothia­zine-3-carboxyl­ate 1,1-dioxide
title_short Methyl 4-eth­oxy-2-methyl-2H-1,2-benzothia­zine-3-carboxyl­ate 1,1-dioxide
title_sort methyl 4-eth­oxy-2-methyl-2h-1,2-benzothia­zine-3-carboxyl­ate 1,1-dioxide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962229/
https://www.ncbi.nlm.nih.gov/pubmed/21203217
http://dx.doi.org/10.1107/S1600536808021363
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AT elsegoodmarkrj methyl4ethoxy2methyl2h12benzothiazine3carboxylate11dioxide
AT akbarnoshin methyl4ethoxy2methyl2h12benzothiazine3carboxylate11dioxide
AT latifsiddiquihamid methyl4ethoxy2methyl2h12benzothiazine3carboxylate11dioxide

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