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N-(4-Chloro-2-nitrophenyl)methanesulfonamide
The title compound, C(7)H(7)ClN(2)O(4)S, is of interest as a precursor to biologically active substituted quinolines. Its structure resembles those of the previously reported N-phenylmethane sulfonamide and its 4-nitro, 4-fluoro and 4-bromo derivatives, with slightly different geometric parameters...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959442/ https://www.ncbi.nlm.nih.gov/pubmed/21201228 http://dx.doi.org/10.1107/S1600536808031048 |
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author | Zia-ur-Rehman, Muhammad Choudary, Jamil Anwar Akbar, Nosheen Khan, Islam Ullah Nadeem Arshad, Muhammad |
author_facet | Zia-ur-Rehman, Muhammad Choudary, Jamil Anwar Akbar, Nosheen Khan, Islam Ullah Nadeem Arshad, Muhammad |
author_sort | Zia-ur-Rehman, Muhammad |
collection | PubMed |
description | The title compound, C(7)H(7)ClN(2)O(4)S, is of interest as a precursor to biologically active substituted quinolines. Its structure resembles those of the previously reported N-phenylmethane sulfonamide and its 4-nitro, 4-fluoro and 4-bromo derivatives, with slightly different geometric parameters. An intramolecular N—H⋯O hydrogen bond gives rise to a six-membered ring. Intermolecular C—H⋯O contacts stabilize the crystal packing. |
format | Text |
id | pubmed-2959442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29594422010-12-30 N-(4-Chloro-2-nitrophenyl)methanesulfonamide Zia-ur-Rehman, Muhammad Choudary, Jamil Anwar Akbar, Nosheen Khan, Islam Ullah Nadeem Arshad, Muhammad Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(7)H(7)ClN(2)O(4)S, is of interest as a precursor to biologically active substituted quinolines. Its structure resembles those of the previously reported N-phenylmethane sulfonamide and its 4-nitro, 4-fluoro and 4-bromo derivatives, with slightly different geometric parameters. An intramolecular N—H⋯O hydrogen bond gives rise to a six-membered ring. Intermolecular C—H⋯O contacts stabilize the crystal packing. International Union of Crystallography 2008-09-30 /pmc/articles/PMC2959442/ /pubmed/21201228 http://dx.doi.org/10.1107/S1600536808031048 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 Akbar, Nosheen Khan, Islam Ullah Nadeem Arshad, Muhammad N-(4-Chloro-2-nitrophenyl)methanesulfonamide |
title |
N-(4-Chloro-2-nitrophenyl)methanesulfonamide |
title_full |
N-(4-Chloro-2-nitrophenyl)methanesulfonamide |
title_fullStr |
N-(4-Chloro-2-nitrophenyl)methanesulfonamide |
title_full_unstemmed |
N-(4-Chloro-2-nitrophenyl)methanesulfonamide |
title_short |
N-(4-Chloro-2-nitrophenyl)methanesulfonamide |
title_sort | n-(4-chloro-2-nitrophenyl)methanesulfonamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959442/ https://www.ncbi.nlm.nih.gov/pubmed/21201228 http://dx.doi.org/10.1107/S1600536808031048 |
work_keys_str_mv | AT ziaurrehmanmuhammad n4chloro2nitrophenylmethanesulfonamide AT choudaryjamilanwar n4chloro2nitrophenylmethanesulfonamide AT akbarnosheen n4chloro2nitrophenylmethanesulfonamide AT khanislamullah n4chloro2nitrophenylmethanesulfonamide AT nadeemarshadmuhammad n4chloro2nitrophenylmethanesulfonamide |