2-Chloro-N-(3-meth­oxy­benzo­yl)benzene­sulfonamide

In the title compound, C(14)H(12)ClNO(4)S, the dihedral angle between the chloro- and meth­oxy-substituted benzene rings is 87.40 (1)°. In the crystal, adjacent mol­ecules form inversion-related dimers through strong N—H⋯O hydrogen bonds, generating R (2) (2)(8) loops. The dimers are further connect...

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Autores principales: Suchetan, P. A., Palakshamurthy, B. S., Mamatha, G. R., Kumar, Vijith, Mohan, N. R., Sreenivasa, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793723/
https://www.ncbi.nlm.nih.gov/pubmed/24109310
http://dx.doi.org/10.1107/S1600536813018291
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author Suchetan, P. A.
Palakshamurthy, B. S.
Mamatha, G. R.
Kumar, Vijith
Mohan, N. R.
Sreenivasa, S.
author_facet Suchetan, P. A.
Palakshamurthy, B. S.
Mamatha, G. R.
Kumar, Vijith
Mohan, N. R.
Sreenivasa, S.
author_sort Suchetan, P. A.
collection PubMed
description In the title compound, C(14)H(12)ClNO(4)S, the dihedral angle between the chloro- and meth­oxy-substituted benzene rings is 87.40 (1)°. In the crystal, adjacent mol­ecules form inversion-related dimers through strong N—H⋯O hydrogen bonds, generating R (2) (2)(8) loops. The dimers are further connected through two C—H⋯O inter­actions that form C(11) chains and R (2) (2)(14) loops. Aromatic π–π stacking inter­actions [centroid–centroid separation = 3.8574 (1) Å] are also observed.
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spelling pubmed-37937232013-10-09 2-Chloro-N-(3-meth­oxy­benzo­yl)benzene­sulfonamide Suchetan, P. A. Palakshamurthy, B. S. Mamatha, G. R. Kumar, Vijith Mohan, N. R. Sreenivasa, S. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(14)H(12)ClNO(4)S, the dihedral angle between the chloro- and meth­oxy-substituted benzene rings is 87.40 (1)°. In the crystal, adjacent mol­ecules form inversion-related dimers through strong N—H⋯O hydrogen bonds, generating R (2) (2)(8) loops. The dimers are further connected through two C—H⋯O inter­actions that form C(11) chains and R (2) (2)(14) loops. Aromatic π–π stacking inter­actions [centroid–centroid separation = 3.8574 (1) Å] are also observed. International Union of Crystallography 2013-07-06 /pmc/articles/PMC3793723/ /pubmed/24109310 http://dx.doi.org/10.1107/S1600536813018291 Text en © Suchetan et al. 2013 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.
Palakshamurthy, B. S.
Mamatha, G. R.
Kumar, Vijith
Mohan, N. R.
Sreenivasa, S.
2-Chloro-N-(3-meth­oxy­benzo­yl)benzene­sulfonamide
title 2-Chloro-N-(3-meth­oxy­benzo­yl)benzene­sulfonamide
title_full 2-Chloro-N-(3-meth­oxy­benzo­yl)benzene­sulfonamide
title_fullStr 2-Chloro-N-(3-meth­oxy­benzo­yl)benzene­sulfonamide
title_full_unstemmed 2-Chloro-N-(3-meth­oxy­benzo­yl)benzene­sulfonamide
title_short 2-Chloro-N-(3-meth­oxy­benzo­yl)benzene­sulfonamide
title_sort 2-chloro-n-(3-meth­oxy­benzo­yl)benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793723/
https://www.ncbi.nlm.nih.gov/pubmed/24109310
http://dx.doi.org/10.1107/S1600536813018291
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AT kumarvijith 2chloron3methoxybenzoylbenzenesulfonamide
AT mohannr 2chloron3methoxybenzoylbenzenesulfonamide
AT sreenivasas 2chloron3methoxybenzoylbenzenesulfonamide

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