Ethyl (E)-3-hy­droxy-2-[(4-meth­oxy­styr­yl)­carbamo­yl]but-2-enoate

The title compound, C(16)H(19)NO(5), which was synthesized from p-meth­oxy­cinnamic acid, has intra­molecular O—H⋯O and N—H⋯O hydrogen-bonding inter­actions. In the crystal, mol­ecules are linked by weak C—H⋯O hydrogen bonds and aromatic π–π stacking inter­actions [minimum ring centroid–centroid sep...

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Detalles Bibliográficos
Autores principales: Zhao, Sheng-Yin, Huang, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297865/
https://www.ncbi.nlm.nih.gov/pubmed/22412668
http://dx.doi.org/10.1107/S1600536812006538
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author Zhao, Sheng-Yin
Huang, Jing
author_facet Zhao, Sheng-Yin
Huang, Jing
author_sort Zhao, Sheng-Yin
collection PubMed
description The title compound, C(16)H(19)NO(5), which was synthesized from p-meth­oxy­cinnamic acid, has intra­molecular O—H⋯O and N—H⋯O hydrogen-bonding inter­actions. In the crystal, mol­ecules are linked by weak C—H⋯O hydrogen bonds and aromatic π–π stacking inter­actions [minimum ring centroid–centroid separation = 3.790 (1) Å].
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spelling pubmed-32978652012-03-12 Ethyl (E)-3-hy­droxy-2-[(4-meth­oxy­styr­yl)­carbamo­yl]but-2-enoate Zhao, Sheng-Yin Huang, Jing Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(16)H(19)NO(5), which was synthesized from p-meth­oxy­cinnamic acid, has intra­molecular O—H⋯O and N—H⋯O hydrogen-bonding inter­actions. In the crystal, mol­ecules are linked by weak C—H⋯O hydrogen bonds and aromatic π–π stacking inter­actions [minimum ring centroid–centroid separation = 3.790 (1) Å]. International Union of Crystallography 2012-02-24 /pmc/articles/PMC3297865/ /pubmed/22412668 http://dx.doi.org/10.1107/S1600536812006538 Text en © Zhao and Huang 2012 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
Zhao, Sheng-Yin
Huang, Jing
Ethyl (E)-3-hy­droxy-2-[(4-meth­oxy­styr­yl)­carbamo­yl]but-2-enoate
title Ethyl (E)-3-hy­droxy-2-[(4-meth­oxy­styr­yl)­carbamo­yl]but-2-enoate
title_full Ethyl (E)-3-hy­droxy-2-[(4-meth­oxy­styr­yl)­carbamo­yl]but-2-enoate
title_fullStr Ethyl (E)-3-hy­droxy-2-[(4-meth­oxy­styr­yl)­carbamo­yl]but-2-enoate
title_full_unstemmed Ethyl (E)-3-hy­droxy-2-[(4-meth­oxy­styr­yl)­carbamo­yl]but-2-enoate
title_short Ethyl (E)-3-hy­droxy-2-[(4-meth­oxy­styr­yl)­carbamo­yl]but-2-enoate
title_sort ethyl (e)-3-hy­droxy-2-[(4-meth­oxy­styr­yl)­carbamo­yl]but-2-enoate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297865/
https://www.ncbi.nlm.nih.gov/pubmed/22412668
http://dx.doi.org/10.1107/S1600536812006538
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AT huangjing ethyle3hydroxy24methoxystyrylcarbamoylbut2enoate

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