4-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 mol­ecule is twisted at the S atom with a torsion angle of 69.0 (2)°. The dihedral angle between the sulfonyl benzene ring and the —SO(2)—NH—C—O segment is 77.2 (1)...

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Detalles Bibliográficos
Autores principales: Suchetan, P. A., Gowda, B. Thimme, Foro, Sabine, 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/PMC2979638/
https://www.ncbi.nlm.nih.gov/pubmed/21579561
http://dx.doi.org/10.1107/S1600536810019501
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author Suchetan, P. A.
Gowda, B. Thimme
Foro, Sabine
Fuess, Hartmut
author_facet Suchetan, P. A.
Gowda, B. Thimme
Foro, Sabine
Fuess, Hartmut
author_sort Suchetan, P. A.
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 mol­ecule is twisted at the S atom with a torsion angle of 69.0 (2)°. The dihedral angle between the sulfonyl benzene ring and the —SO(2)—NH—C—O segment is 77.2 (1)° and that between the sulfonyl and the benzoyl benzene rings is 89.5 (1)°. In the structure, mol­ecules are linked into chains via N—H⋯O hydrogen bonds, forming inversion dimers.
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spelling pubmed-29796382010-12-30 4-Chloro-N-(4-methyl­benzo­yl)benzene­sulfonamide Suchetan, P. A. Gowda, B. Thimme Foro, Sabine 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 mol­ecule is twisted at the S atom with a torsion angle of 69.0 (2)°. The dihedral angle between the sulfonyl benzene ring and the —SO(2)—NH—C—O segment is 77.2 (1)° and that between the sulfonyl and the benzoyl benzene rings is 89.5 (1)°. In the structure, mol­ecules are linked into chains via N—H⋯O hydrogen bonds, forming inversion dimers. International Union of Crystallography 2010-05-29 /pmc/articles/PMC2979638/ /pubmed/21579561 http://dx.doi.org/10.1107/S1600536810019501 Text en © Suchetan 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
Suchetan, P. A.
Gowda, B. Thimme
Foro, Sabine
Fuess, Hartmut
4-Chloro-N-(4-methyl­benzo­yl)benzene­sulfonamide
title 4-Chloro-N-(4-methyl­benzo­yl)benzene­sulfonamide
title_full 4-Chloro-N-(4-methyl­benzo­yl)benzene­sulfonamide
title_fullStr 4-Chloro-N-(4-methyl­benzo­yl)benzene­sulfonamide
title_full_unstemmed 4-Chloro-N-(4-methyl­benzo­yl)benzene­sulfonamide
title_short 4-Chloro-N-(4-methyl­benzo­yl)benzene­sulfonamide
title_sort 4-chloro-n-(4-methyl­benzo­yl)benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979638/
https://www.ncbi.nlm.nih.gov/pubmed/21579561
http://dx.doi.org/10.1107/S1600536810019501
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AT gowdabthimme 4chloron4methylbenzoylbenzenesulfonamide
AT forosabine 4chloron4methylbenzoylbenzenesulfonamide
AT fuesshartmut 4chloron4methylbenzoylbenzenesulfonamide

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