1,3-Dimethyl-2,6-diphenyl­piperidin-4-one

In the title moleclue, C(19)H(21)NO, the 4-piperidone ring adopts a chair conformation in which the two benzene rings and the methyl group attached to C atoms all have equatorial orientations. In the crystal structure, centrosymmetric dimers are formed through weak inter­molecular C—H⋯O hydrogen bon...

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Autores principales: Nithya, P., Hathwar, Venkatesha R., Maiyalagan, T., Kazak, Canan, Nawaz Khan, F.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968156/
https://www.ncbi.nlm.nih.gov/pubmed/21582024
http://dx.doi.org/10.1107/S1600536809003419
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author Nithya, P.
Hathwar, Venkatesha R.
Maiyalagan, T.
Kazak, Canan
Nawaz Khan, F.
author_facet Nithya, P.
Hathwar, Venkatesha R.
Maiyalagan, T.
Kazak, Canan
Nawaz Khan, F.
author_sort Nithya, P.
collection PubMed
description In the title moleclue, C(19)H(21)NO, the 4-piperidone ring adopts a chair conformation in which the two benzene rings and the methyl group attached to C atoms all have equatorial orientations. In the crystal structure, centrosymmetric dimers are formed through weak inter­molecular C—H⋯O hydrogen bonds [the dihedral angle between the aromatic rings is 58.51 (5)°].
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spelling pubmed-29681562010-12-30 1,3-Dimethyl-2,6-diphenyl­piperidin-4-one Nithya, P. Hathwar, Venkatesha R. Maiyalagan, T. Kazak, Canan Nawaz Khan, F. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title moleclue, C(19)H(21)NO, the 4-piperidone ring adopts a chair conformation in which the two benzene rings and the methyl group attached to C atoms all have equatorial orientations. In the crystal structure, centrosymmetric dimers are formed through weak inter­molecular C—H⋯O hydrogen bonds [the dihedral angle between the aromatic rings is 58.51 (5)°]. International Union of Crystallography 2009-01-31 /pmc/articles/PMC2968156/ /pubmed/21582024 http://dx.doi.org/10.1107/S1600536809003419 Text en © Nithya 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
Nithya, P.
Hathwar, Venkatesha R.
Maiyalagan, T.
Kazak, Canan
Nawaz Khan, F.
1,3-Dimethyl-2,6-diphenyl­piperidin-4-one
title 1,3-Dimethyl-2,6-diphenyl­piperidin-4-one
title_full 1,3-Dimethyl-2,6-diphenyl­piperidin-4-one
title_fullStr 1,3-Dimethyl-2,6-diphenyl­piperidin-4-one
title_full_unstemmed 1,3-Dimethyl-2,6-diphenyl­piperidin-4-one
title_short 1,3-Dimethyl-2,6-diphenyl­piperidin-4-one
title_sort 1,3-dimethyl-2,6-diphenyl­piperidin-4-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968156/
https://www.ncbi.nlm.nih.gov/pubmed/21582024
http://dx.doi.org/10.1107/S1600536809003419
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AT hathwarvenkateshar 13dimethyl26diphenylpiperidin4one
AT maiyalagant 13dimethyl26diphenylpiperidin4one
AT kazakcanan 13dimethyl26diphenylpiperidin4one
AT nawazkhanf 13dimethyl26diphenylpiperidin4one

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