Cargando…

N-(3-Chloro­benzo­yl)benzene­sulfonamide

In the crystal structure of the title compound, C(13)H(10)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 two benzene rings is 87.5 (1)°. The crystal structure features inversion-related dimers linked by pairs of N—H⋯O...

Descripción completa

Detalles Bibliográficos
Autores principales: Gowda, B. Thimme, Foro, Sabine, Suchetan, P. A., Fuess, Hartmut
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971321/
https://www.ncbi.nlm.nih.gov/pubmed/21578344
http://dx.doi.org/10.1107/S1600536809041051
_version_ 1782190599487619072
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 crystal structure of the title compound, C(13)H(10)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 two benzene rings is 87.5 (1)°. The crystal structure features inversion-related dimers linked by pairs of N—H⋯O(S) hydrogen bonds.
format Text
id pubmed-2971321
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29713212010-12-30 N-(3-Chloro­benzo­yl)benzene­sulfonamide Gowda, B. Thimme Foro, Sabine Suchetan, P. A. Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(13)H(10)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 two benzene rings is 87.5 (1)°. The crystal structure features inversion-related dimers linked by pairs of N—H⋯O(S) hydrogen bonds. International Union of Crystallography 2009-10-17 /pmc/articles/PMC2971321/ /pubmed/21578344 http://dx.doi.org/10.1107/S1600536809041051 Text en © Gowda et al. 2009 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
N-(3-Chloro­benzo­yl)benzene­sulfonamide
title N-(3-Chloro­benzo­yl)benzene­sulfonamide
title_full N-(3-Chloro­benzo­yl)benzene­sulfonamide
title_fullStr N-(3-Chloro­benzo­yl)benzene­sulfonamide
title_full_unstemmed N-(3-Chloro­benzo­yl)benzene­sulfonamide
title_short N-(3-Chloro­benzo­yl)benzene­sulfonamide
title_sort n-(3-chloro­benzo­yl)benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971321/
https://www.ncbi.nlm.nih.gov/pubmed/21578344
http://dx.doi.org/10.1107/S1600536809041051
work_keys_str_mv AT gowdabthimme n3chlorobenzoylbenzenesulfonamide
AT forosabine n3chlorobenzoylbenzenesulfonamide
AT suchetanpa n3chlorobenzoylbenzenesulfonamide
AT fuesshartmut n3chlorobenzoylbenzenesulfonamide