2-Methyl-N-(3-methyl­benzo­yl)benzene­sulfonamide

In the title compound, C(15)H(15)NO(3)S, the sulfonyl and amide-bound benzene rings are oriented at dihedral angles of 83.1 (1) and 22.5 (3)°, respectively, with the almost planar S—N—C=O segment (r.m.s. deviation = 0.003 Å). The dihedral angle between the two benzene rings is 74.8 (1)°. In the crys...

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Detalles Bibliográficos
Autores principales: Gowda, B. Thimme, Foro, Sabine, Suchetan, P. A., 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/PMC2979884/
https://www.ncbi.nlm.nih.gov/pubmed/21579848
http://dx.doi.org/10.1107/S1600536810002254
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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 title compound, C(15)H(15)NO(3)S, the sulfonyl and amide-bound benzene rings are oriented at dihedral angles of 83.1 (1) and 22.5 (3)°, respectively, with the almost planar S—N—C=O segment (r.m.s. deviation = 0.003 Å). The dihedral angle between the two benzene rings is 74.8 (1)°. In the crystal structure, pairs of mol­ecules are linked into centrosymmetric dimers by pairs of N—H⋯O hydrogen bonds.
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spelling pubmed-29798842010-12-30 2-Methyl-N-(3-methyl­benzo­yl)benzene­sulfonamide Gowda, B. Thimme Foro, Sabine Suchetan, P. A. Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(15)NO(3)S, the sulfonyl and amide-bound benzene rings are oriented at dihedral angles of 83.1 (1) and 22.5 (3)°, respectively, with the almost planar S—N—C=O segment (r.m.s. deviation = 0.003 Å). The dihedral angle between the two benzene rings is 74.8 (1)°. In the crystal structure, pairs of mol­ecules are linked into centrosymmetric dimers by pairs of N—H⋯O hydrogen bonds. International Union of Crystallography 2010-01-23 /pmc/articles/PMC2979884/ /pubmed/21579848 http://dx.doi.org/10.1107/S1600536810002254 Text en © Gowda 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
Gowda, B. Thimme
Foro, Sabine
Suchetan, P. A.
Fuess, Hartmut
2-Methyl-N-(3-methyl­benzo­yl)benzene­sulfonamide
title 2-Methyl-N-(3-methyl­benzo­yl)benzene­sulfonamide
title_full 2-Methyl-N-(3-methyl­benzo­yl)benzene­sulfonamide
title_fullStr 2-Methyl-N-(3-methyl­benzo­yl)benzene­sulfonamide
title_full_unstemmed 2-Methyl-N-(3-methyl­benzo­yl)benzene­sulfonamide
title_short 2-Methyl-N-(3-methyl­benzo­yl)benzene­sulfonamide
title_sort 2-methyl-n-(3-methyl­benzo­yl)benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979884/
https://www.ncbi.nlm.nih.gov/pubmed/21579848
http://dx.doi.org/10.1107/S1600536810002254
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AT forosabine 2methyln3methylbenzoylbenzenesulfonamide
AT suchetanpa 2methyln3methylbenzoylbenzenesulfonamide
AT fuesshartmut 2methyln3methylbenzoylbenzenesulfonamide

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