N-(3-Chloro­benzo­yl)-2-methyl­benzene­sulfonamide

In the title compound, C(14)H(12)ClNO(3)S, the N—H bond in the C—SO(2)—NH—C(O) segment is anti to the C=O bond. Further, the C=O bond and the meta-Cl atom in the benzoyl ring are also anti to each other. The dihedral angle between the sulfonyl and the benzoyl benzene rings is 72.4 (1)°. In the cryst...

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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 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3239113/
https://www.ncbi.nlm.nih.gov/pubmed/22199961
http://dx.doi.org/10.1107/S1600536811050574
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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 N—H bond in the C—SO(2)—NH—C(O) segment is anti to the C=O bond. Further, the C=O bond and the meta-Cl atom in the benzoyl ring are also anti to each other. The dihedral angle between the sulfonyl and the benzoyl benzene rings is 72.4 (1)°. In the crystal, mol­ecules are linked by pairs of N—H⋯O hydrogen bonds, forming inversion dimers.
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spelling pubmed-32391132011-12-23 N-(3-Chloro­benzo­yl)-2-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 N—H bond in the C—SO(2)—NH—C(O) segment is anti to the C=O bond. Further, the C=O bond and the meta-Cl atom in the benzoyl ring are also anti to each other. The dihedral angle between the sulfonyl and the benzoyl benzene rings is 72.4 (1)°. In the crystal, mol­ecules are linked by pairs of N—H⋯O hydrogen bonds, forming inversion dimers. International Union of Crystallography 2011-11-30 /pmc/articles/PMC3239113/ /pubmed/22199961 http://dx.doi.org/10.1107/S1600536811050574 Text en © Suchetan et al. 2011 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-(3-Chloro­benzo­yl)-2-methyl­benzene­sulfonamide
title N-(3-Chloro­benzo­yl)-2-methyl­benzene­sulfonamide
title_full N-(3-Chloro­benzo­yl)-2-methyl­benzene­sulfonamide
title_fullStr N-(3-Chloro­benzo­yl)-2-methyl­benzene­sulfonamide
title_full_unstemmed N-(3-Chloro­benzo­yl)-2-methyl­benzene­sulfonamide
title_short N-(3-Chloro­benzo­yl)-2-methyl­benzene­sulfonamide
title_sort n-(3-chloro­benzo­yl)-2-methyl­benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3239113/
https://www.ncbi.nlm.nih.gov/pubmed/22199961
http://dx.doi.org/10.1107/S1600536811050574
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AT forosabine n3chlorobenzoyl2methylbenzenesulfonamide
AT gowdabthimme n3chlorobenzoyl2methylbenzenesulfonamide

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