N,N′-Bis(3,4-dimethoxy­benzyl­idene)butane-1,4-diamine

The title Schiff base compound, C(22)H(28)N(2)O(4), was synthesized by the reaction of 3,4-dimethoxy­benzaldehyde and 1,4-diamino­butane in methanol. The mol­ecule is located on a center of inversion with one half-mol­ecule in the asymmetric unit. Both C=N double bonds are in a trans configuration....

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Detalles Bibliográficos
Autores principales: Dehno Khalaji, Aliakbar, Fejfarova, Karla, Dusek, Michal
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977286/
https://www.ncbi.nlm.nih.gov/pubmed/21583481
http://dx.doi.org/10.1107/S1600536809025069
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author Dehno Khalaji, Aliakbar
Fejfarova, Karla
Dusek, Michal
author_facet Dehno Khalaji, Aliakbar
Fejfarova, Karla
Dusek, Michal
author_sort Dehno Khalaji, Aliakbar
collection PubMed
description The title Schiff base compound, C(22)H(28)N(2)O(4), was synthesized by the reaction of 3,4-dimethoxy­benzaldehyde and 1,4-diamino­butane in methanol. The mol­ecule is located on a center of inversion with one half-mol­ecule in the asymmetric unit. Both C=N double bonds are in a trans configuration. Inter­molecular C—H⋯O hydrogen bonds link the mol­ecules into a three-dimensional network.
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spelling pubmed-29772862010-12-30 N,N′-Bis(3,4-dimethoxy­benzyl­idene)butane-1,4-diamine Dehno Khalaji, Aliakbar Fejfarova, Karla Dusek, Michal Acta Crystallogr Sect E Struct Rep Online Organic Papers The title Schiff base compound, C(22)H(28)N(2)O(4), was synthesized by the reaction of 3,4-dimethoxy­benzaldehyde and 1,4-diamino­butane in methanol. The mol­ecule is located on a center of inversion with one half-mol­ecule in the asymmetric unit. Both C=N double bonds are in a trans configuration. Inter­molecular C—H⋯O hydrogen bonds link the mol­ecules into a three-dimensional network. International Union of Crystallography 2009-07-04 /pmc/articles/PMC2977286/ /pubmed/21583481 http://dx.doi.org/10.1107/S1600536809025069 Text en © Dehno Khalaji et al. 2009 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
Dehno Khalaji, Aliakbar
Fejfarova, Karla
Dusek, Michal
N,N′-Bis(3,4-dimethoxy­benzyl­idene)butane-1,4-diamine
title N,N′-Bis(3,4-dimethoxy­benzyl­idene)butane-1,4-diamine
title_full N,N′-Bis(3,4-dimethoxy­benzyl­idene)butane-1,4-diamine
title_fullStr N,N′-Bis(3,4-dimethoxy­benzyl­idene)butane-1,4-diamine
title_full_unstemmed N,N′-Bis(3,4-dimethoxy­benzyl­idene)butane-1,4-diamine
title_short N,N′-Bis(3,4-dimethoxy­benzyl­idene)butane-1,4-diamine
title_sort n,n′-bis(3,4-dimethoxy­benzyl­idene)butane-1,4-diamine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977286/
https://www.ncbi.nlm.nih.gov/pubmed/21583481
http://dx.doi.org/10.1107/S1600536809025069
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AT fejfarovakarla nnbis34dimethoxybenzylidenebutane14diamine
AT dusekmichal nnbis34dimethoxybenzylidenebutane14diamine

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