r-2,c-6-Bis(4-chloro­phen­yl)-c-3,t-3-dimethyl­piperidin-4-one

In the title mol­ecule, C(19)H(19)Cl(2)NO, the piperidine ring adopts a chair conformation and the dihedral angle between the two benzene rings is 77.23 (7)°. In the crystal structure, mol­ecules are linked by N—H⋯O and C—H⋯O hydrogen bonds, and a weak C—H⋯π inter­action is also observed....

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Detalles Bibliográficos
Autores principales: Ilango, S. S., Ponnuswamy, S., Gayathri, P., Thiruvalluvar, A., Butcher, R. J.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960012/
https://www.ncbi.nlm.nih.gov/pubmed/21581289
http://dx.doi.org/10.1107/S1600536808036325
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author Ilango, S. S.
Ponnuswamy, S.
Gayathri, P.
Thiruvalluvar, A.
Butcher, R. J.
author_facet Ilango, S. S.
Ponnuswamy, S.
Gayathri, P.
Thiruvalluvar, A.
Butcher, R. J.
author_sort Ilango, S. S.
collection PubMed
description In the title mol­ecule, C(19)H(19)Cl(2)NO, the piperidine ring adopts a chair conformation and the dihedral angle between the two benzene rings is 77.23 (7)°. In the crystal structure, mol­ecules are linked by N—H⋯O and C—H⋯O hydrogen bonds, and a weak C—H⋯π inter­action is also observed.
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spelling pubmed-29600122010-12-30 r-2,c-6-Bis(4-chloro­phen­yl)-c-3,t-3-dimethyl­piperidin-4-one Ilango, S. S. Ponnuswamy, S. Gayathri, P. Thiruvalluvar, A. Butcher, R. J. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title mol­ecule, C(19)H(19)Cl(2)NO, the piperidine ring adopts a chair conformation and the dihedral angle between the two benzene rings is 77.23 (7)°. In the crystal structure, mol­ecules are linked by N—H⋯O and C—H⋯O hydrogen bonds, and a weak C—H⋯π inter­action is also observed. International Union of Crystallography 2008-11-13 /pmc/articles/PMC2960012/ /pubmed/21581289 http://dx.doi.org/10.1107/S1600536808036325 Text en © Ilango 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
Ilango, S. S.
Ponnuswamy, S.
Gayathri, P.
Thiruvalluvar, A.
Butcher, R. J.
r-2,c-6-Bis(4-chloro­phen­yl)-c-3,t-3-dimethyl­piperidin-4-one
title r-2,c-6-Bis(4-chloro­phen­yl)-c-3,t-3-dimethyl­piperidin-4-one
title_full r-2,c-6-Bis(4-chloro­phen­yl)-c-3,t-3-dimethyl­piperidin-4-one
title_fullStr r-2,c-6-Bis(4-chloro­phen­yl)-c-3,t-3-dimethyl­piperidin-4-one
title_full_unstemmed r-2,c-6-Bis(4-chloro­phen­yl)-c-3,t-3-dimethyl­piperidin-4-one
title_short r-2,c-6-Bis(4-chloro­phen­yl)-c-3,t-3-dimethyl­piperidin-4-one
title_sort r-2,c-6-bis(4-chloro­phen­yl)-c-3,t-3-dimethyl­piperidin-4-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960012/
https://www.ncbi.nlm.nih.gov/pubmed/21581289
http://dx.doi.org/10.1107/S1600536808036325
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AT thiruvalluvara r2c6bis4chlorophenylc3t3dimethylpiperidin4one
AT butcherrj r2c6bis4chlorophenylc3t3dimethylpiperidin4one

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