2-(Benzene­sulfonamido)acetic acid

The title compound, C(8)H(9)NO(4)S, is of inter­est as a precursor to biologically active sulfur-containing heterocyclic cmpounds. The crystal structure displays the classical O—H⋯O inter­molecular hydrogen bonding typical for carboxylic acids forming dimers. Symmetry-related dimers are, in turn, li...

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Detalles Bibliográficos
Autores principales: Arshad, Muhammad Nadeem, Khan, Islam Ullah, Zia-ur-Rehman, Muhammad
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959830/
https://www.ncbi.nlm.nih.gov/pubmed/21581263
http://dx.doi.org/10.1107/S1600536808035721
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author Arshad, Muhammad Nadeem
Khan, Islam Ullah
Zia-ur-Rehman, Muhammad
author_facet Arshad, Muhammad Nadeem
Khan, Islam Ullah
Zia-ur-Rehman, Muhammad
author_sort Arshad, Muhammad Nadeem
collection PubMed
description The title compound, C(8)H(9)NO(4)S, is of inter­est as a precursor to biologically active sulfur-containing heterocyclic cmpounds. The crystal structure displays the classical O—H⋯O inter­molecular hydrogen bonding typical for carboxylic acids forming dimers. Symmetry-related dimers are, in turn, linked through head-to-tail pairs of inter­molecular N—H⋯O inter­actions, giving rise to a zigzag chain along the c axis.
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spelling pubmed-29598302010-12-30 2-(Benzene­sulfonamido)acetic acid Arshad, Muhammad Nadeem Khan, Islam Ullah Zia-ur-Rehman, Muhammad Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(8)H(9)NO(4)S, is of inter­est as a precursor to biologically active sulfur-containing heterocyclic cmpounds. The crystal structure displays the classical O—H⋯O inter­molecular hydrogen bonding typical for carboxylic acids forming dimers. Symmetry-related dimers are, in turn, linked through head-to-tail pairs of inter­molecular N—H⋯O inter­actions, giving rise to a zigzag chain along the c axis. International Union of Crystallography 2008-11-08 /pmc/articles/PMC2959830/ /pubmed/21581263 http://dx.doi.org/10.1107/S1600536808035721 Text en © Arshad 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
Arshad, Muhammad Nadeem
Khan, Islam Ullah
Zia-ur-Rehman, Muhammad
2-(Benzene­sulfonamido)acetic acid
title 2-(Benzene­sulfonamido)acetic acid
title_full 2-(Benzene­sulfonamido)acetic acid
title_fullStr 2-(Benzene­sulfonamido)acetic acid
title_full_unstemmed 2-(Benzene­sulfonamido)acetic acid
title_short 2-(Benzene­sulfonamido)acetic acid
title_sort 2-(benzene­sulfonamido)acetic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959830/
https://www.ncbi.nlm.nih.gov/pubmed/21581263
http://dx.doi.org/10.1107/S1600536808035721
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