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1-Allyl-3-phenyl­quinoxalin-2(1H)-one

The title compound, C(17)H(14)N(2)O, crystallizes with two mol­ecules in the asymmetric unit. The dihedral angles between the mean planes of the quinoxaline ring system and the phenyl ring in the two mol­ecules are 38.27 (10) and 37.14 (8)°. In the crystal, π-stacking along the b axis contributes to...

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Detalles Bibliográficos
Autores principales: Benzeid, Hanane, Bouhfid, Rachid, Massip, Stephane, Leger, Jean Michel, Essassi, El Mokhtar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247392/
https://www.ncbi.nlm.nih.gov/pubmed/22220010
http://dx.doi.org/10.1107/S1600536811042474
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author Benzeid, Hanane
Bouhfid, Rachid
Massip, Stephane
Leger, Jean Michel
Essassi, El Mokhtar
author_facet Benzeid, Hanane
Bouhfid, Rachid
Massip, Stephane
Leger, Jean Michel
Essassi, El Mokhtar
author_sort Benzeid, Hanane
collection PubMed
description The title compound, C(17)H(14)N(2)O, crystallizes with two mol­ecules in the asymmetric unit. The dihedral angles between the mean planes of the quinoxaline ring system and the phenyl ring in the two mol­ecules are 38.27 (10) and 37.14 (8)°. In the crystal, π-stacking along the b axis contributes to the crystal cohesion with an average distance between quinoxaline units of 3.397 (3) Å. Weak C—H⋯O interactions also occur.
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spelling pubmed-32473922012-01-04 1-Allyl-3-phenyl­quinoxalin-2(1H)-one Benzeid, Hanane Bouhfid, Rachid Massip, Stephane Leger, Jean Michel Essassi, El Mokhtar Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(17)H(14)N(2)O, crystallizes with two mol­ecules in the asymmetric unit. The dihedral angles between the mean planes of the quinoxaline ring system and the phenyl ring in the two mol­ecules are 38.27 (10) and 37.14 (8)°. In the crystal, π-stacking along the b axis contributes to the crystal cohesion with an average distance between quinoxaline units of 3.397 (3) Å. Weak C—H⋯O interactions also occur. International Union of Crystallography 2011-10-22 /pmc/articles/PMC3247392/ /pubmed/22220010 http://dx.doi.org/10.1107/S1600536811042474 Text en © Benzeid et al. 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
Benzeid, Hanane
Bouhfid, Rachid
Massip, Stephane
Leger, Jean Michel
Essassi, El Mokhtar
1-Allyl-3-phenyl­quinoxalin-2(1H)-one
title 1-Allyl-3-phenyl­quinoxalin-2(1H)-one
title_full 1-Allyl-3-phenyl­quinoxalin-2(1H)-one
title_fullStr 1-Allyl-3-phenyl­quinoxalin-2(1H)-one
title_full_unstemmed 1-Allyl-3-phenyl­quinoxalin-2(1H)-one
title_short 1-Allyl-3-phenyl­quinoxalin-2(1H)-one
title_sort 1-allyl-3-phenyl­quinoxalin-2(1h)-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247392/
https://www.ncbi.nlm.nih.gov/pubmed/22220010
http://dx.doi.org/10.1107/S1600536811042474
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