N-(4-Hydroxy­phen­yl)benzene­sulfon­amide

The title compound, C(12)H(11)NO(3)S, synthesized by the reaction of benzene sulfonyl chloride with para-amino­phenol, is of inter­est as a precursor to biologically active sulfur-containing heterocyclic compounds. The structure is stabilized by N—H⋯O and O—H⋯O hydrogen bonds.

Detalles Bibliográficos
Autores principales: Khan, Islam Ullah, Mariam, Irfana, Zia-ur-Rehman, Muhammad, Arif Sajjad, Muhammad, Sharif, Shahzad
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979209/
https://www.ncbi.nlm.nih.gov/pubmed/21579141
http://dx.doi.org/10.1107/S160053681001322X
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author Khan, Islam Ullah
Mariam, Irfana
Zia-ur-Rehman, Muhammad
Arif Sajjad, Muhammad
Sharif, Shahzad
author_facet Khan, Islam Ullah
Mariam, Irfana
Zia-ur-Rehman, Muhammad
Arif Sajjad, Muhammad
Sharif, Shahzad
author_sort Khan, Islam Ullah
collection PubMed
description The title compound, C(12)H(11)NO(3)S, synthesized by the reaction of benzene sulfonyl chloride with para-amino­phenol, is of inter­est as a precursor to biologically active sulfur-containing heterocyclic compounds. The structure is stabilized by N—H⋯O and O—H⋯O hydrogen bonds.
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spelling pubmed-29792092010-12-30 N-(4-Hydroxy­phen­yl)benzene­sulfon­amide Khan, Islam Ullah Mariam, Irfana Zia-ur-Rehman, Muhammad Arif Sajjad, Muhammad Sharif, Shahzad Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(12)H(11)NO(3)S, synthesized by the reaction of benzene sulfonyl chloride with para-amino­phenol, is of inter­est as a precursor to biologically active sulfur-containing heterocyclic compounds. The structure is stabilized by N—H⋯O and O—H⋯O hydrogen bonds. International Union of Crystallography 2010-04-14 /pmc/articles/PMC2979209/ /pubmed/21579141 http://dx.doi.org/10.1107/S160053681001322X Text en © Khan 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
Khan, Islam Ullah
Mariam, Irfana
Zia-ur-Rehman, Muhammad
Arif Sajjad, Muhammad
Sharif, Shahzad
N-(4-Hydroxy­phen­yl)benzene­sulfon­amide
title N-(4-Hydroxy­phen­yl)benzene­sulfon­amide
title_full N-(4-Hydroxy­phen­yl)benzene­sulfon­amide
title_fullStr N-(4-Hydroxy­phen­yl)benzene­sulfon­amide
title_full_unstemmed N-(4-Hydroxy­phen­yl)benzene­sulfon­amide
title_short N-(4-Hydroxy­phen­yl)benzene­sulfon­amide
title_sort n-(4-hydroxy­phen­yl)benzene­sulfon­amide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979209/
https://www.ncbi.nlm.nih.gov/pubmed/21579141
http://dx.doi.org/10.1107/S160053681001322X
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AT mariamirfana n4hydroxyphenylbenzenesulfonamide
AT ziaurrehmanmuhammad n4hydroxyphenylbenzenesulfonamide
AT arifsajjadmuhammad n4hydroxyphenylbenzenesulfonamide
AT sharifshahzad n4hydroxyphenylbenzenesulfonamide

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