N-(2-Chloro­benzo­yl)-4-methyl­benzene­sulfonamide

In the title compound, C(14)H(12)ClNO(3)S, the C=O bond is syn to the Cl substituent in the adjacent benzene ring. The C—S—N—C torsion angle is −80.6 (6)°. The chloro­benzoyl ring is disordered and was refined using a split model [occupancy ratio 0.537 (3):0.463 (3)]. In the crystal, mol­ecules are...

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Detalles Bibliográficos
Autores principales: Suchetan, P. A., Foro, Sabine, Gowda, B. Thimme
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344529/
https://www.ncbi.nlm.nih.gov/pubmed/22590291
http://dx.doi.org/10.1107/S1600536812015681
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author Suchetan, P. A.
Foro, Sabine
Gowda, B. Thimme
author_facet Suchetan, P. A.
Foro, Sabine
Gowda, B. Thimme
author_sort Suchetan, P. A.
collection PubMed
description In the title compound, C(14)H(12)ClNO(3)S, the C=O bond is syn to the Cl substituent in the adjacent benzene ring. The C—S—N—C torsion angle is −80.6 (6)°. The chloro­benzoyl ring is disordered and was refined using a split model [occupancy ratio 0.537 (3):0.463 (3)]. In the crystal, mol­ecules are linked by pairs of N—H⋯O(S) hydrogen bonds, forming inversion dimers.
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spelling pubmed-33445292012-05-15 N-(2-Chloro­benzo­yl)-4-methyl­benzene­sulfonamide Suchetan, P. A. Foro, Sabine Gowda, B. Thimme Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(14)H(12)ClNO(3)S, the C=O bond is syn to the Cl substituent in the adjacent benzene ring. The C—S—N—C torsion angle is −80.6 (6)°. The chloro­benzoyl ring is disordered and was refined using a split model [occupancy ratio 0.537 (3):0.463 (3)]. In the crystal, mol­ecules are linked by pairs of N—H⋯O(S) hydrogen bonds, forming inversion dimers. International Union of Crystallography 2012-04-18 /pmc/articles/PMC3344529/ /pubmed/22590291 http://dx.doi.org/10.1107/S1600536812015681 Text en © Suchetan et al. 2012 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.
Foro, Sabine
Gowda, B. Thimme
N-(2-Chloro­benzo­yl)-4-methyl­benzene­sulfonamide
title N-(2-Chloro­benzo­yl)-4-methyl­benzene­sulfonamide
title_full N-(2-Chloro­benzo­yl)-4-methyl­benzene­sulfonamide
title_fullStr N-(2-Chloro­benzo­yl)-4-methyl­benzene­sulfonamide
title_full_unstemmed N-(2-Chloro­benzo­yl)-4-methyl­benzene­sulfonamide
title_short N-(2-Chloro­benzo­yl)-4-methyl­benzene­sulfonamide
title_sort n-(2-chloro­benzo­yl)-4-methyl­benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344529/
https://www.ncbi.nlm.nih.gov/pubmed/22590291
http://dx.doi.org/10.1107/S1600536812015681
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AT gowdabthimme n2chlorobenzoyl4methylbenzenesulfonamide

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