2-Chloro-N-(4-methyl­benzo­yl)benzene­sulfonamide

In the title compound, C(14)H(12)ClNO(3)S, the conformation of the N—H bond in the C—SO(2)—NH—C(O) segment is anti to the C=O bond. The dihedral angle between the sulfonyl benzene ring and the —SO(2)—NH—C—O segment is 89.4 (1)° and that between the sulfonyl and benzoyl benzene rings is 89.1 (2)°. Th...

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Detalles Bibliográficos
Autores principales: Gowda, B. Thimme, Foro, Sabine, Suchetan, P. A., Fuess, Hartmut
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979447/
https://www.ncbi.nlm.nih.gov/pubmed/21579534
http://dx.doi.org/10.1107/S1600536810018908
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author Gowda, B. Thimme
Foro, Sabine
Suchetan, P. A.
Fuess, Hartmut
author_facet Gowda, B. Thimme
Foro, Sabine
Suchetan, P. A.
Fuess, Hartmut
author_sort Gowda, B. Thimme
collection PubMed
description In the title compound, C(14)H(12)ClNO(3)S, the conformation of the N—H bond in the C—SO(2)—NH—C(O) segment is anti to the C=O bond. The dihedral angle between the sulfonyl benzene ring and the —SO(2)—NH—C—O segment is 89.4 (1)° and that between the sulfonyl and benzoyl benzene rings is 89.1 (2)°. The crystal structure features inversion-related dimers linked by pairs of N—H⋯O hydrogen bonds.
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spelling pubmed-29794472010-12-30 2-Chloro-N-(4-methyl­benzo­yl)benzene­sulfonamide Gowda, B. Thimme Foro, Sabine Suchetan, P. A. Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(14)H(12)ClNO(3)S, the conformation of the N—H bond in the C—SO(2)—NH—C(O) segment is anti to the C=O bond. The dihedral angle between the sulfonyl benzene ring and the —SO(2)—NH—C—O segment is 89.4 (1)° and that between the sulfonyl and benzoyl benzene rings is 89.1 (2)°. The crystal structure features inversion-related dimers linked by pairs of N—H⋯O hydrogen bonds. International Union of Crystallography 2010-05-26 /pmc/articles/PMC2979447/ /pubmed/21579534 http://dx.doi.org/10.1107/S1600536810018908 Text en © Gowda 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
Gowda, B. Thimme
Foro, Sabine
Suchetan, P. A.
Fuess, Hartmut
2-Chloro-N-(4-methyl­benzo­yl)benzene­sulfonamide
title 2-Chloro-N-(4-methyl­benzo­yl)benzene­sulfonamide
title_full 2-Chloro-N-(4-methyl­benzo­yl)benzene­sulfonamide
title_fullStr 2-Chloro-N-(4-methyl­benzo­yl)benzene­sulfonamide
title_full_unstemmed 2-Chloro-N-(4-methyl­benzo­yl)benzene­sulfonamide
title_short 2-Chloro-N-(4-methyl­benzo­yl)benzene­sulfonamide
title_sort 2-chloro-n-(4-methyl­benzo­yl)benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979447/
https://www.ncbi.nlm.nih.gov/pubmed/21579534
http://dx.doi.org/10.1107/S1600536810018908
work_keys_str_mv AT gowdabthimme 2chloron4methylbenzoylbenzenesulfonamide
AT forosabine 2chloron4methylbenzoylbenzenesulfonamide
AT suchetanpa 2chloron4methylbenzoylbenzenesulfonamide
AT fuesshartmut 2chloron4methylbenzoylbenzenesulfonamide

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