Cargando…
1,4-Bis(4-tert-butylbenzyl)piperazine
The complete molecule of the title compound, C(26)H(38)N(2), is generated by a crystallographic inversion centre. The piperazine ring adopts a chair conformation with pseudo-equatorial substituents. In the crystal, molecules interact only by van der Waals forces.
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247480/ https://www.ncbi.nlm.nih.gov/pubmed/22220098 http://dx.doi.org/10.1107/S1600536811044114 |
_version_ | 1782220116811841536 |
---|---|
author | Luo, Li-Juan Weng, Jian-Quan |
author_facet | Luo, Li-Juan Weng, Jian-Quan |
author_sort | Luo, Li-Juan |
collection | PubMed |
description | The complete molecule of the title compound, C(26)H(38)N(2), is generated by a crystallographic inversion centre. The piperazine ring adopts a chair conformation with pseudo-equatorial substituents. In the crystal, molecules interact only by van der Waals forces. |
format | Online Article Text |
id | pubmed-3247480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32474802012-01-04 1,4-Bis(4-tert-butylbenzyl)piperazine Luo, Li-Juan Weng, Jian-Quan Acta Crystallogr Sect E Struct Rep Online Organic Papers The complete molecule of the title compound, C(26)H(38)N(2), is generated by a crystallographic inversion centre. The piperazine ring adopts a chair conformation with pseudo-equatorial substituents. In the crystal, molecules interact only by van der Waals forces. International Union of Crystallography 2011-10-29 /pmc/articles/PMC3247480/ /pubmed/22220098 http://dx.doi.org/10.1107/S1600536811044114 Text en © Luo and Weng 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 Luo, Li-Juan Weng, Jian-Quan 1,4-Bis(4-tert-butylbenzyl)piperazine |
title | 1,4-Bis(4-tert-butylbenzyl)piperazine |
title_full | 1,4-Bis(4-tert-butylbenzyl)piperazine |
title_fullStr | 1,4-Bis(4-tert-butylbenzyl)piperazine |
title_full_unstemmed | 1,4-Bis(4-tert-butylbenzyl)piperazine |
title_short | 1,4-Bis(4-tert-butylbenzyl)piperazine |
title_sort | 1,4-bis(4-tert-butylbenzyl)piperazine |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247480/ https://www.ncbi.nlm.nih.gov/pubmed/22220098 http://dx.doi.org/10.1107/S1600536811044114 |
work_keys_str_mv | AT luolijuan 14bis4tertbutylbenzylpiperazine AT wengjianquan 14bis4tertbutylbenzylpiperazine |