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Methyl (E)-2-({2-[(E)-(hy­droxy­imino)­meth­yl]phen­oxy}meth­yl)-3-phenyl­acrylate

In the title compound, C(18)H(17)NO(4), the hy­droxy­ethanimine group is essentially coplanar with the ring to which it is attached [C—C—N—O torsion angle = 179.94 (14)°]. The mol­ecules are linked into cyclic centrosymmetric R (2) (2)(6) dimers via O—H⋯N hydrogen bonds and the crystal packing is fu...

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Autores principales: Suresh, G., Sabari, V., Srinivasan, J., Mannickam, Bakthadoss, Aravindhan, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295410/
https://www.ncbi.nlm.nih.gov/pubmed/22412521
http://dx.doi.org/10.1107/S1600536812002711
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author Suresh, G.
Sabari, V.
Srinivasan, J.
Mannickam, Bakthadoss
Aravindhan, S.
author_facet Suresh, G.
Sabari, V.
Srinivasan, J.
Mannickam, Bakthadoss
Aravindhan, S.
author_sort Suresh, G.
collection PubMed
description In the title compound, C(18)H(17)NO(4), the hy­droxy­ethanimine group is essentially coplanar with the ring to which it is attached [C—C—N—O torsion angle = 179.94 (14)°]. The mol­ecules are linked into cyclic centrosymmetric R (2) (2)(6) dimers via O—H⋯N hydrogen bonds and the crystal packing is further stabilized by C—H⋯O inter­actions.
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spelling pubmed-32954102012-03-12 Methyl (E)-2-({2-[(E)-(hy­droxy­imino)­meth­yl]phen­oxy}meth­yl)-3-phenyl­acrylate Suresh, G. Sabari, V. Srinivasan, J. Mannickam, Bakthadoss Aravindhan, S. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(18)H(17)NO(4), the hy­droxy­ethanimine group is essentially coplanar with the ring to which it is attached [C—C—N—O torsion angle = 179.94 (14)°]. The mol­ecules are linked into cyclic centrosymmetric R (2) (2)(6) dimers via O—H⋯N hydrogen bonds and the crystal packing is further stabilized by C—H⋯O inter­actions. International Union of Crystallography 2012-02-04 /pmc/articles/PMC3295410/ /pubmed/22412521 http://dx.doi.org/10.1107/S1600536812002711 Text en © Suresh et al. 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
Suresh, G.
Sabari, V.
Srinivasan, J.
Mannickam, Bakthadoss
Aravindhan, S.
Methyl (E)-2-({2-[(E)-(hy­droxy­imino)­meth­yl]phen­oxy}meth­yl)-3-phenyl­acrylate
title Methyl (E)-2-({2-[(E)-(hy­droxy­imino)­meth­yl]phen­oxy}meth­yl)-3-phenyl­acrylate
title_full Methyl (E)-2-({2-[(E)-(hy­droxy­imino)­meth­yl]phen­oxy}meth­yl)-3-phenyl­acrylate
title_fullStr Methyl (E)-2-({2-[(E)-(hy­droxy­imino)­meth­yl]phen­oxy}meth­yl)-3-phenyl­acrylate
title_full_unstemmed Methyl (E)-2-({2-[(E)-(hy­droxy­imino)­meth­yl]phen­oxy}meth­yl)-3-phenyl­acrylate
title_short Methyl (E)-2-({2-[(E)-(hy­droxy­imino)­meth­yl]phen­oxy}meth­yl)-3-phenyl­acrylate
title_sort methyl (e)-2-({2-[(e)-(hy­droxy­imino)­meth­yl]phen­oxy}meth­yl)-3-phenyl­acrylate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295410/
https://www.ncbi.nlm.nih.gov/pubmed/22412521
http://dx.doi.org/10.1107/S1600536812002711
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