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2,6-Bis(3-fluoro­phen­yl)-3-isopropyl­piperidin-4-one

In the title compound, C(20)H(21)F(2)NO, the piperidine ring in each of the two independent mol­ecules in the asymmetric unit adopts a normal chair conformation with an equatorial orientation of the 3-fluoro­phenyl groups. The dihedral angles between the two 3-fluoro­phenyl rings are 49.89 (7) and 5...

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Detalles Bibliográficos
Autores principales: Ramachandran, R., Rani, M., Kabilan, S., Jeong, Yeon Tae
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007008/
https://www.ncbi.nlm.nih.gov/pubmed/21588057
http://dx.doi.org/10.1107/S1600536810024414
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author Ramachandran, R.
Rani, M.
Kabilan, S.
Jeong, Yeon Tae
author_facet Ramachandran, R.
Rani, M.
Kabilan, S.
Jeong, Yeon Tae
author_sort Ramachandran, R.
collection PubMed
description In the title compound, C(20)H(21)F(2)NO, the piperidine ring in each of the two independent mol­ecules in the asymmetric unit adopts a normal chair conformation with an equatorial orientation of the 3-fluoro­phenyl groups. The dihedral angles between the two 3-fluoro­phenyl rings are 49.89 (7) and 50.35 (7)° in the two mol­ecules.
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spelling pubmed-30070082010-12-30 2,6-Bis(3-fluoro­phen­yl)-3-isopropyl­piperidin-4-one Ramachandran, R. Rani, M. Kabilan, S. Jeong, Yeon Tae Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(20)H(21)F(2)NO, the piperidine ring in each of the two independent mol­ecules in the asymmetric unit adopts a normal chair conformation with an equatorial orientation of the 3-fluoro­phenyl groups. The dihedral angles between the two 3-fluoro­phenyl rings are 49.89 (7) and 50.35 (7)° in the two mol­ecules. International Union of Crystallography 2010-06-30 /pmc/articles/PMC3007008/ /pubmed/21588057 http://dx.doi.org/10.1107/S1600536810024414 Text en © Ramachandran 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
Ramachandran, R.
Rani, M.
Kabilan, S.
Jeong, Yeon Tae
2,6-Bis(3-fluoro­phen­yl)-3-isopropyl­piperidin-4-one
title 2,6-Bis(3-fluoro­phen­yl)-3-isopropyl­piperidin-4-one
title_full 2,6-Bis(3-fluoro­phen­yl)-3-isopropyl­piperidin-4-one
title_fullStr 2,6-Bis(3-fluoro­phen­yl)-3-isopropyl­piperidin-4-one
title_full_unstemmed 2,6-Bis(3-fluoro­phen­yl)-3-isopropyl­piperidin-4-one
title_short 2,6-Bis(3-fluoro­phen­yl)-3-isopropyl­piperidin-4-one
title_sort 2,6-bis(3-fluoro­phen­yl)-3-isopropyl­piperidin-4-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007008/
https://www.ncbi.nlm.nih.gov/pubmed/21588057
http://dx.doi.org/10.1107/S1600536810024414
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AT jeongyeontae 26bis3fluorophenyl3isopropylpiperidin4one