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2-Chloro-4,6-bis­(piperidin-1-yl)-1,3,5-triazine

The title compound, C(13)H(20)ClN(5), crystallizes with two mol­ecules in the asymmetric unit. The piperidine rings in both mol­ecules adopt chair conformations. Weak π–π inter­actions [centroid–centroid distance = 3.9815 (8) Å] are observed in the crystal structure.

Detalles Bibliográficos
Autores principales: Vennila, Jasmine P., Thiruvadigal, D. John, Kavitha, Helen P., Chakkaravarthi, G., Manivannan, V.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051665/
https://www.ncbi.nlm.nih.gov/pubmed/21523000
http://dx.doi.org/10.1107/S1600536811000584
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author Vennila, Jasmine P.
Thiruvadigal, D. John
Kavitha, Helen P.
Chakkaravarthi, G.
Manivannan, V.
author_facet Vennila, Jasmine P.
Thiruvadigal, D. John
Kavitha, Helen P.
Chakkaravarthi, G.
Manivannan, V.
author_sort Vennila, Jasmine P.
collection PubMed
description The title compound, C(13)H(20)ClN(5), crystallizes with two mol­ecules in the asymmetric unit. The piperidine rings in both mol­ecules adopt chair conformations. Weak π–π inter­actions [centroid–centroid distance = 3.9815 (8) Å] are observed in the crystal structure.
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spelling pubmed-30516652011-04-26 2-Chloro-4,6-bis­(piperidin-1-yl)-1,3,5-triazine Vennila, Jasmine P. Thiruvadigal, D. John Kavitha, Helen P. Chakkaravarthi, G. Manivannan, V. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(13)H(20)ClN(5), crystallizes with two mol­ecules in the asymmetric unit. The piperidine rings in both mol­ecules adopt chair conformations. Weak π–π inter­actions [centroid–centroid distance = 3.9815 (8) Å] are observed in the crystal structure. International Union of Crystallography 2011-01-08 /pmc/articles/PMC3051665/ /pubmed/21523000 http://dx.doi.org/10.1107/S1600536811000584 Text en © Vennila et al. 2011 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
Vennila, Jasmine P.
Thiruvadigal, D. John
Kavitha, Helen P.
Chakkaravarthi, G.
Manivannan, V.
2-Chloro-4,6-bis­(piperidin-1-yl)-1,3,5-triazine
title 2-Chloro-4,6-bis­(piperidin-1-yl)-1,3,5-triazine
title_full 2-Chloro-4,6-bis­(piperidin-1-yl)-1,3,5-triazine
title_fullStr 2-Chloro-4,6-bis­(piperidin-1-yl)-1,3,5-triazine
title_full_unstemmed 2-Chloro-4,6-bis­(piperidin-1-yl)-1,3,5-triazine
title_short 2-Chloro-4,6-bis­(piperidin-1-yl)-1,3,5-triazine
title_sort 2-chloro-4,6-bis­(piperidin-1-yl)-1,3,5-triazine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051665/
https://www.ncbi.nlm.nih.gov/pubmed/21523000
http://dx.doi.org/10.1107/S1600536811000584
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