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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.
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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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. |
format | Text |
id | pubmed-3051665 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
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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