Methyl 2-allyl-4-hydr­oxy-2H-1,2-benzothia­zine-3-carboxyl­ate 1,1-dioxide

In the title compound, C(13)H(13)NO(5)S, the thia­zine ring adopts a distorted half-chair conformation. Intra­molecular O—H⋯O and C—H⋯O hydrogen bonds give rise to two six-membered hydrogen bonded rings. In the crystal, mol­ecules are linked through weak inter­molecular C—H⋯O hydrogen bonds, resulti...

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Detalles Bibliográficos
Autores principales: Arshad, Muhammad Nadeem, Zia-ur-Rehman, Muhammad, Khan, Islam Ullah
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971956/
https://www.ncbi.nlm.nih.gov/pubmed/21578807
http://dx.doi.org/10.1107/S160053680904673X
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author Arshad, Muhammad Nadeem
Zia-ur-Rehman, Muhammad
Khan, Islam Ullah
author_facet Arshad, Muhammad Nadeem
Zia-ur-Rehman, Muhammad
Khan, Islam Ullah
author_sort Arshad, Muhammad Nadeem
collection PubMed
description In the title compound, C(13)H(13)NO(5)S, the thia­zine ring adopts a distorted half-chair conformation. Intra­molecular O—H⋯O and C—H⋯O hydrogen bonds give rise to two six-membered hydrogen bonded rings. In the crystal, mol­ecules are linked through weak inter­molecular C—H⋯O hydrogen bonds, resulting in a zigzag chain lying along the c axis.
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spelling pubmed-29719562010-12-30 Methyl 2-allyl-4-hydr­oxy-2H-1,2-benzothia­zine-3-carboxyl­ate 1,1-dioxide Arshad, Muhammad Nadeem Zia-ur-Rehman, Muhammad Khan, Islam Ullah Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(13)NO(5)S, the thia­zine ring adopts a distorted half-chair conformation. Intra­molecular O—H⋯O and C—H⋯O hydrogen bonds give rise to two six-membered hydrogen bonded rings. In the crystal, mol­ecules are linked through weak inter­molecular C—H⋯O hydrogen bonds, resulting in a zigzag chain lying along the c axis. International Union of Crystallography 2009-11-14 /pmc/articles/PMC2971956/ /pubmed/21578807 http://dx.doi.org/10.1107/S160053680904673X Text en © Arshad 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
Arshad, Muhammad Nadeem
Zia-ur-Rehman, Muhammad
Khan, Islam Ullah
Methyl 2-allyl-4-hydr­oxy-2H-1,2-benzothia­zine-3-carboxyl­ate 1,1-dioxide
title Methyl 2-allyl-4-hydr­oxy-2H-1,2-benzothia­zine-3-carboxyl­ate 1,1-dioxide
title_full Methyl 2-allyl-4-hydr­oxy-2H-1,2-benzothia­zine-3-carboxyl­ate 1,1-dioxide
title_fullStr Methyl 2-allyl-4-hydr­oxy-2H-1,2-benzothia­zine-3-carboxyl­ate 1,1-dioxide
title_full_unstemmed Methyl 2-allyl-4-hydr­oxy-2H-1,2-benzothia­zine-3-carboxyl­ate 1,1-dioxide
title_short Methyl 2-allyl-4-hydr­oxy-2H-1,2-benzothia­zine-3-carboxyl­ate 1,1-dioxide
title_sort methyl 2-allyl-4-hydr­oxy-2h-1,2-benzothia­zine-3-carboxyl­ate 1,1-dioxide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971956/
https://www.ncbi.nlm.nih.gov/pubmed/21578807
http://dx.doi.org/10.1107/S160053680904673X
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AT khanislamullah methyl2allyl4hydroxy2h12benzothiazine3carboxylate11dioxide

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