(N (1) E,N (2) E)-N (1),N (2)-Bis(4-hex­yloxy-3-methoxy­benzyl­idene)ethane-1,2-diamine

The title compound, C(30)H(44)N(2)O(4), was obtained from the dimerization of 4-hexyl­oxyvanillin with ethyl­enediamine in 95% methanol solution. It adopts a trans configuration with respect to the C=N bond and possesses a crystallographically imposed centre of symmetry.

Detalles Bibliográficos
Autores principales: Paul, Anju, Punnoose, Sherin Susan, Mary, N. L., Narasimhaswamy, T., Ramkumar, V.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979600/
https://www.ncbi.nlm.nih.gov/pubmed/21579458
http://dx.doi.org/10.1107/S1600536810017125
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author Paul, Anju
Punnoose, Sherin Susan
Mary, N. L.
Narasimhaswamy, T.
Ramkumar, V.
author_facet Paul, Anju
Punnoose, Sherin Susan
Mary, N. L.
Narasimhaswamy, T.
Ramkumar, V.
author_sort Paul, Anju
collection PubMed
description The title compound, C(30)H(44)N(2)O(4), was obtained from the dimerization of 4-hexyl­oxyvanillin with ethyl­enediamine in 95% methanol solution. It adopts a trans configuration with respect to the C=N bond and possesses a crystallographically imposed centre of symmetry.
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spelling pubmed-29796002010-12-30 (N (1) E,N (2) E)-N (1),N (2)-Bis(4-hex­yloxy-3-methoxy­benzyl­idene)ethane-1,2-diamine Paul, Anju Punnoose, Sherin Susan Mary, N. L. Narasimhaswamy, T. Ramkumar, V. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(30)H(44)N(2)O(4), was obtained from the dimerization of 4-hexyl­oxyvanillin with ethyl­enediamine in 95% methanol solution. It adopts a trans configuration with respect to the C=N bond and possesses a crystallographically imposed centre of symmetry. International Union of Crystallography 2010-05-19 /pmc/articles/PMC2979600/ /pubmed/21579458 http://dx.doi.org/10.1107/S1600536810017125 Text en © Paul 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
Paul, Anju
Punnoose, Sherin Susan
Mary, N. L.
Narasimhaswamy, T.
Ramkumar, V.
(N (1) E,N (2) E)-N (1),N (2)-Bis(4-hex­yloxy-3-methoxy­benzyl­idene)ethane-1,2-diamine
title (N (1) E,N (2) E)-N (1),N (2)-Bis(4-hex­yloxy-3-methoxy­benzyl­idene)ethane-1,2-diamine
title_full (N (1) E,N (2) E)-N (1),N (2)-Bis(4-hex­yloxy-3-methoxy­benzyl­idene)ethane-1,2-diamine
title_fullStr (N (1) E,N (2) E)-N (1),N (2)-Bis(4-hex­yloxy-3-methoxy­benzyl­idene)ethane-1,2-diamine
title_full_unstemmed (N (1) E,N (2) E)-N (1),N (2)-Bis(4-hex­yloxy-3-methoxy­benzyl­idene)ethane-1,2-diamine
title_short (N (1) E,N (2) E)-N (1),N (2)-Bis(4-hex­yloxy-3-methoxy­benzyl­idene)ethane-1,2-diamine
title_sort (n (1) e,n (2) e)-n (1),n (2)-bis(4-hex­yloxy-3-methoxy­benzyl­idene)ethane-1,2-diamine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979600/
https://www.ncbi.nlm.nih.gov/pubmed/21579458
http://dx.doi.org/10.1107/S1600536810017125
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AT ramkumarv n1en2en1n2bis4hexyloxy3methoxybenzylideneethane12diamine

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