Ethyl 2-[2-(2-meth­oxy­phen­yl)hydrazinyl­idene]-3-oxobutano­ate

In the title compound, C(13)H(16)N(2)O(4), an intra­molecular N—H⋯O hydrogen bond generates an S(6) ring. The mol­ecule adopts an E configuration with respect to the central C=N double bond. In the crystal, symmetry-related mol­ecules are connected into chains along [010] via weak C—H⋯N hydrogen bon...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Hemamalini, Madhukar, Shetty, Shobhitha, Kalluraya, BalaKrishna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201242/
https://www.ncbi.nlm.nih.gov/pubmed/22058737
http://dx.doi.org/10.1107/S1600536811034854
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author Fun, Hoong-Kun
Hemamalini, Madhukar
Shetty, Shobhitha
Kalluraya, BalaKrishna
author_facet Fun, Hoong-Kun
Hemamalini, Madhukar
Shetty, Shobhitha
Kalluraya, BalaKrishna
author_sort Fun, Hoong-Kun
collection PubMed
description In the title compound, C(13)H(16)N(2)O(4), an intra­molecular N—H⋯O hydrogen bond generates an S(6) ring. The mol­ecule adopts an E configuration with respect to the central C=N double bond. In the crystal, symmetry-related mol­ecules are connected into chains along [010] via weak C—H⋯N hydrogen bonds. The crystal structure is further stabilized by weak C—H⋯π inter­actions.
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spelling pubmed-32012422011-11-06 Ethyl 2-[2-(2-meth­oxy­phen­yl)hydrazinyl­idene]-3-oxobutano­ate Fun, Hoong-Kun Hemamalini, Madhukar Shetty, Shobhitha Kalluraya, BalaKrishna Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(16)N(2)O(4), an intra­molecular N—H⋯O hydrogen bond generates an S(6) ring. The mol­ecule adopts an E configuration with respect to the central C=N double bond. In the crystal, symmetry-related mol­ecules are connected into chains along [010] via weak C—H⋯N hydrogen bonds. The crystal structure is further stabilized by weak C—H⋯π inter­actions. International Union of Crystallography 2011-09-14 /pmc/articles/PMC3201242/ /pubmed/22058737 http://dx.doi.org/10.1107/S1600536811034854 Text en © Fun 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
Fun, Hoong-Kun
Hemamalini, Madhukar
Shetty, Shobhitha
Kalluraya, BalaKrishna
Ethyl 2-[2-(2-meth­oxy­phen­yl)hydrazinyl­idene]-3-oxobutano­ate
title Ethyl 2-[2-(2-meth­oxy­phen­yl)hydrazinyl­idene]-3-oxobutano­ate
title_full Ethyl 2-[2-(2-meth­oxy­phen­yl)hydrazinyl­idene]-3-oxobutano­ate
title_fullStr Ethyl 2-[2-(2-meth­oxy­phen­yl)hydrazinyl­idene]-3-oxobutano­ate
title_full_unstemmed Ethyl 2-[2-(2-meth­oxy­phen­yl)hydrazinyl­idene]-3-oxobutano­ate
title_short Ethyl 2-[2-(2-meth­oxy­phen­yl)hydrazinyl­idene]-3-oxobutano­ate
title_sort ethyl 2-[2-(2-meth­oxy­phen­yl)hydrazinyl­idene]-3-oxobutano­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201242/
https://www.ncbi.nlm.nih.gov/pubmed/22058737
http://dx.doi.org/10.1107/S1600536811034854
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