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2,3-Bis(4-ethoxy­phen­yl)quinoxaline

The title compound, C(24)H(22)N(2)O(2), was prepared by condensation of 1,2-bis­(4-ethoxy­phen­yl)ethane-1,2-dione and 1,2-diamino­benzene. The asymmetric unit contains one half-mol­ecule, close to a twofold axis. The plane of the quinoxaline ring is twisted with respect to the planes of the two eth...

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Detalles Bibliográficos
Autores principales: Ye, Ping-Ping, Zhang, Cai-Li, Du, Zhi-Qiang
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980160/
https://www.ncbi.nlm.nih.gov/pubmed/21580021
http://dx.doi.org/10.1107/S1600536809052295
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author Ye, Ping-Ping
Zhang, Cai-Li
Du, Zhi-Qiang
author_facet Ye, Ping-Ping
Zhang, Cai-Li
Du, Zhi-Qiang
author_sort Ye, Ping-Ping
collection PubMed
description The title compound, C(24)H(22)N(2)O(2), was prepared by condensation of 1,2-bis­(4-ethoxy­phen­yl)ethane-1,2-dione and 1,2-diamino­benzene. The asymmetric unit contains one half-mol­ecule, close to a twofold axis. The plane of the quinoxaline ring is twisted with respect to the planes of the two ethoxy­phenyl ring systems, exhibiting dihedral angles of 39.95 (9)°. The crystal packing is dominated by weak C—H⋯π inter­actions. No classical hydrogen bonds or stacking inter­actions are observed.
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spelling pubmed-29801602010-12-30 2,3-Bis(4-ethoxy­phen­yl)quinoxaline Ye, Ping-Ping Zhang, Cai-Li Du, Zhi-Qiang Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(24)H(22)N(2)O(2), was prepared by condensation of 1,2-bis­(4-ethoxy­phen­yl)ethane-1,2-dione and 1,2-diamino­benzene. The asymmetric unit contains one half-mol­ecule, close to a twofold axis. The plane of the quinoxaline ring is twisted with respect to the planes of the two ethoxy­phenyl ring systems, exhibiting dihedral angles of 39.95 (9)°. The crystal packing is dominated by weak C—H⋯π inter­actions. No classical hydrogen bonds or stacking inter­actions are observed. International Union of Crystallography 2009-12-12 /pmc/articles/PMC2980160/ /pubmed/21580021 http://dx.doi.org/10.1107/S1600536809052295 Text en © Ye 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
Ye, Ping-Ping
Zhang, Cai-Li
Du, Zhi-Qiang
2,3-Bis(4-ethoxy­phen­yl)quinoxaline
title 2,3-Bis(4-ethoxy­phen­yl)quinoxaline
title_full 2,3-Bis(4-ethoxy­phen­yl)quinoxaline
title_fullStr 2,3-Bis(4-ethoxy­phen­yl)quinoxaline
title_full_unstemmed 2,3-Bis(4-ethoxy­phen­yl)quinoxaline
title_short 2,3-Bis(4-ethoxy­phen­yl)quinoxaline
title_sort 2,3-bis(4-ethoxy­phen­yl)quinoxaline
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980160/
https://www.ncbi.nlm.nih.gov/pubmed/21580021
http://dx.doi.org/10.1107/S1600536809052295
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