(1R,2R)-N,N′-Bis[1-(2-pyrid­yl)ethyl­idene]cyclo­hexane-1,2-diamine

In the title compound, C(20)H(24)N(4), the cyclo­hexane ring adopts a chair conformation with the two imine groups linked at equatorial positions. The two halves of the mol­ecule are related by a crystallographic twofold rotation axis. The dihedral angle between the pyridine rings is 75.73 (3)°....

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Detalles Bibliográficos
Autores principales: Saleh Salga, Muhammad, Khaledi, Hamid, Mohd Ali, Hapipah, Puteh, Rustam
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979034/
https://www.ncbi.nlm.nih.gov/pubmed/21579148
http://dx.doi.org/10.1107/S1600536810013607
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author Saleh Salga, Muhammad
Khaledi, Hamid
Mohd Ali, Hapipah
Puteh, Rustam
author_facet Saleh Salga, Muhammad
Khaledi, Hamid
Mohd Ali, Hapipah
Puteh, Rustam
author_sort Saleh Salga, Muhammad
collection PubMed
description In the title compound, C(20)H(24)N(4), the cyclo­hexane ring adopts a chair conformation with the two imine groups linked at equatorial positions. The two halves of the mol­ecule are related by a crystallographic twofold rotation axis. The dihedral angle between the pyridine rings is 75.73 (3)°.
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spelling pubmed-29790342010-12-30 (1R,2R)-N,N′-Bis[1-(2-pyrid­yl)ethyl­idene]cyclo­hexane-1,2-diamine Saleh Salga, Muhammad Khaledi, Hamid Mohd Ali, Hapipah Puteh, Rustam Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(20)H(24)N(4), the cyclo­hexane ring adopts a chair conformation with the two imine groups linked at equatorial positions. The two halves of the mol­ecule are related by a crystallographic twofold rotation axis. The dihedral angle between the pyridine rings is 75.73 (3)°. International Union of Crystallography 2010-04-17 /pmc/articles/PMC2979034/ /pubmed/21579148 http://dx.doi.org/10.1107/S1600536810013607 Text en © Saleh Salga 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
Saleh Salga, Muhammad
Khaledi, Hamid
Mohd Ali, Hapipah
Puteh, Rustam
(1R,2R)-N,N′-Bis[1-(2-pyrid­yl)ethyl­idene]cyclo­hexane-1,2-diamine
title (1R,2R)-N,N′-Bis[1-(2-pyrid­yl)ethyl­idene]cyclo­hexane-1,2-diamine
title_full (1R,2R)-N,N′-Bis[1-(2-pyrid­yl)ethyl­idene]cyclo­hexane-1,2-diamine
title_fullStr (1R,2R)-N,N′-Bis[1-(2-pyrid­yl)ethyl­idene]cyclo­hexane-1,2-diamine
title_full_unstemmed (1R,2R)-N,N′-Bis[1-(2-pyrid­yl)ethyl­idene]cyclo­hexane-1,2-diamine
title_short (1R,2R)-N,N′-Bis[1-(2-pyrid­yl)ethyl­idene]cyclo­hexane-1,2-diamine
title_sort (1r,2r)-n,n′-bis[1-(2-pyrid­yl)ethyl­idene]cyclo­hexane-1,2-diamine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979034/
https://www.ncbi.nlm.nih.gov/pubmed/21579148
http://dx.doi.org/10.1107/S1600536810013607
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