Crystal structure of 1-methane­sulfonyl-1,2,3,4-tetra­hydro­quinoline

In the title compound, C(10)H(13)NO(2)S, the heterocyclic ring adopts a half-chair conformation and the bond-angle sum at the N atom is 347.9°. In the crystal, inversion dimers linked by pairs of C—H⋯O hydrogen bonds generate R (2) (2)(8) loops.

Detalles Bibliográficos
Autores principales: Jeyaseelan, S., Nagendra Babu, S. L., Venkateshappa, G., Raghavendra Kumar, P., Palakshamurthy, B. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2015
Materias:
Data Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4331909/
https://www.ncbi.nlm.nih.gov/pubmed/25705484
http://dx.doi.org/10.1107/S2056989014025353
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author Jeyaseelan, S.
Nagendra Babu, S. L.
Venkateshappa, G.
Raghavendra Kumar, P.
Palakshamurthy, B. S.
author_facet Jeyaseelan, S.
Nagendra Babu, S. L.
Venkateshappa, G.
Raghavendra Kumar, P.
Palakshamurthy, B. S.
author_sort Jeyaseelan, S.
collection PubMed
description In the title compound, C(10)H(13)NO(2)S, the heterocyclic ring adopts a half-chair conformation and the bond-angle sum at the N atom is 347.9°. In the crystal, inversion dimers linked by pairs of C—H⋯O hydrogen bonds generate R (2) (2)(8) loops.
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spelling pubmed-43319092015-02-20 Crystal structure of 1-methane­sulfonyl-1,2,3,4-tetra­hydro­quinoline Jeyaseelan, S. Nagendra Babu, S. L. Venkateshappa, G. Raghavendra Kumar, P. Palakshamurthy, B. S. Acta Crystallogr E Crystallogr Commun Data Reports In the title compound, C(10)H(13)NO(2)S, the heterocyclic ring adopts a half-chair conformation and the bond-angle sum at the N atom is 347.9°. In the crystal, inversion dimers linked by pairs of C—H⋯O hydrogen bonds generate R (2) (2)(8) loops. International Union of Crystallography 2015-01-01 /pmc/articles/PMC4331909/ /pubmed/25705484 http://dx.doi.org/10.1107/S2056989014025353 Text en © Jeyaseelan et al. 2015 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 Data Reports
Jeyaseelan, S.
Nagendra Babu, S. L.
Venkateshappa, G.
Raghavendra Kumar, P.
Palakshamurthy, B. S.
Crystal structure of 1-methane­sulfonyl-1,2,3,4-tetra­hydro­quinoline
title Crystal structure of 1-methane­sulfonyl-1,2,3,4-tetra­hydro­quinoline
title_full Crystal structure of 1-methane­sulfonyl-1,2,3,4-tetra­hydro­quinoline
title_fullStr Crystal structure of 1-methane­sulfonyl-1,2,3,4-tetra­hydro­quinoline
title_full_unstemmed Crystal structure of 1-methane­sulfonyl-1,2,3,4-tetra­hydro­quinoline
title_short Crystal structure of 1-methane­sulfonyl-1,2,3,4-tetra­hydro­quinoline
title_sort crystal structure of 1-methane­sulfonyl-1,2,3,4-tetra­hydro­quinoline
topic Data Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4331909/
https://www.ncbi.nlm.nih.gov/pubmed/25705484
http://dx.doi.org/10.1107/S2056989014025353
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