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N-[(E)-1,3-Benzodioxol-5-yl­methyl­idene]-3,4-dimethyl-1,2-oxazol-5-amine

In the title compound, C(13)H(12)N(2)O(3), the dihedral angle between the aromatic rings is 7.94 (12)°. In the crystal, inversion dimers linked by pairs of C—H⋯O hydrogen bonds generate R (2) (2)(6) loops. Weak π–π [centroid–centroid separations = 3.7480 (13) and 3.9047 (13) Å] and C—H⋯π inter­actio...

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Detalles Bibliográficos
Autores principales: Asiri, Abdullah M., Khan, Salman A., Tahir, M. Nawaz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200615/
https://www.ncbi.nlm.nih.gov/pubmed/22058939
http://dx.doi.org/10.1107/S1600536811030327
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author Asiri, Abdullah M.
Khan, Salman A.
Tahir, M. Nawaz
author_facet Asiri, Abdullah M.
Khan, Salman A.
Tahir, M. Nawaz
author_sort Asiri, Abdullah M.
collection PubMed
description In the title compound, C(13)H(12)N(2)O(3), the dihedral angle between the aromatic rings is 7.94 (12)°. In the crystal, inversion dimers linked by pairs of C—H⋯O hydrogen bonds generate R (2) (2)(6) loops. Weak π–π [centroid–centroid separations = 3.7480 (13) and 3.9047 (13) Å] and C—H⋯π inter­actions help to consolidate the packing.
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spelling pubmed-32006152011-11-06 N-[(E)-1,3-Benzodioxol-5-yl­methyl­idene]-3,4-dimethyl-1,2-oxazol-5-amine Asiri, Abdullah M. Khan, Salman A. Tahir, M. Nawaz Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(12)N(2)O(3), the dihedral angle between the aromatic rings is 7.94 (12)°. In the crystal, inversion dimers linked by pairs of C—H⋯O hydrogen bonds generate R (2) (2)(6) loops. Weak π–π [centroid–centroid separations = 3.7480 (13) and 3.9047 (13) Å] and C—H⋯π inter­actions help to consolidate the packing. International Union of Crystallography 2011-08-11 /pmc/articles/PMC3200615/ /pubmed/22058939 http://dx.doi.org/10.1107/S1600536811030327 Text en © Asiri 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
Asiri, Abdullah M.
Khan, Salman A.
Tahir, M. Nawaz
N-[(E)-1,3-Benzodioxol-5-yl­methyl­idene]-3,4-dimethyl-1,2-oxazol-5-amine
title N-[(E)-1,3-Benzodioxol-5-yl­methyl­idene]-3,4-dimethyl-1,2-oxazol-5-amine
title_full N-[(E)-1,3-Benzodioxol-5-yl­methyl­idene]-3,4-dimethyl-1,2-oxazol-5-amine
title_fullStr N-[(E)-1,3-Benzodioxol-5-yl­methyl­idene]-3,4-dimethyl-1,2-oxazol-5-amine
title_full_unstemmed N-[(E)-1,3-Benzodioxol-5-yl­methyl­idene]-3,4-dimethyl-1,2-oxazol-5-amine
title_short N-[(E)-1,3-Benzodioxol-5-yl­methyl­idene]-3,4-dimethyl-1,2-oxazol-5-amine
title_sort n-[(e)-1,3-benzodioxol-5-yl­methyl­idene]-3,4-dimethyl-1,2-oxazol-5-amine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200615/
https://www.ncbi.nlm.nih.gov/pubmed/22058939
http://dx.doi.org/10.1107/S1600536811030327
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