2,2,2-Trimethyl-N-(4-methyl­phenyl­sulfon­yl)acetamide

The bond parameters and conformations of the N—H and C=O bonds of the SO(2)—NH—CO—C group in the title compound, C(12)H(17)NO(3)S, anti to each other, are similar to what has been observed in related structures. The benzene ring and the SO(2)—NH—CO—C group make a dihedral angle of 71.2 (1)°. Inter­m...

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Detalles Bibliográficos
Autores principales: Gowda, B. Thimme, Foro, Sabine, Sowmya, B. P., Nirmala, P. G., Fuess, Hartmut
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961849/
https://www.ncbi.nlm.nih.gov/pubmed/21202906
http://dx.doi.org/10.1107/S1600536808017790
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author Gowda, B. Thimme
Foro, Sabine
Sowmya, B. P.
Nirmala, P. G.
Fuess, Hartmut
author_facet Gowda, B. Thimme
Foro, Sabine
Sowmya, B. P.
Nirmala, P. G.
Fuess, Hartmut
author_sort Gowda, B. Thimme
collection PubMed
description The bond parameters and conformations of the N—H and C=O bonds of the SO(2)—NH—CO—C group in the title compound, C(12)H(17)NO(3)S, anti to each other, are similar to what has been observed in related structures. The benzene ring and the SO(2)—NH—CO—C group make a dihedral angle of 71.2 (1)°. Inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into centrosymmetric dimers.
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spelling pubmed-29618492010-12-30 2,2,2-Trimethyl-N-(4-methyl­phenyl­sulfon­yl)acetamide Gowda, B. Thimme Foro, Sabine Sowmya, B. P. Nirmala, P. G. Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers The bond parameters and conformations of the N—H and C=O bonds of the SO(2)—NH—CO—C group in the title compound, C(12)H(17)NO(3)S, anti to each other, are similar to what has been observed in related structures. The benzene ring and the SO(2)—NH—CO—C group make a dihedral angle of 71.2 (1)°. Inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into centrosymmetric dimers. International Union of Crystallography 2008-06-19 /pmc/articles/PMC2961849/ /pubmed/21202906 http://dx.doi.org/10.1107/S1600536808017790 Text en © Gowda et al. 2008 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
Sowmya, B. P.
Nirmala, P. G.
Fuess, Hartmut
2,2,2-Trimethyl-N-(4-methyl­phenyl­sulfon­yl)acetamide
title 2,2,2-Trimethyl-N-(4-methyl­phenyl­sulfon­yl)acetamide
title_full 2,2,2-Trimethyl-N-(4-methyl­phenyl­sulfon­yl)acetamide
title_fullStr 2,2,2-Trimethyl-N-(4-methyl­phenyl­sulfon­yl)acetamide
title_full_unstemmed 2,2,2-Trimethyl-N-(4-methyl­phenyl­sulfon­yl)acetamide
title_short 2,2,2-Trimethyl-N-(4-methyl­phenyl­sulfon­yl)acetamide
title_sort 2,2,2-trimethyl-n-(4-methyl­phenyl­sulfon­yl)acetamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961849/
https://www.ncbi.nlm.nih.gov/pubmed/21202906
http://dx.doi.org/10.1107/S1600536808017790
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