4-[(E)-(4-Eth­oxy­benzyl­idene)amino]­phenol

The mol­ecule of the title compound, C(15)H(15)NO(2), adopts a trans conformation with respect to the methyl­idene C=N bond and is twisted with a dihedral angle of 26.31 (5)° between the two substituted benzene rings. The eth­oxy group is almost coplanar with the bound benzene ring with a C—O—C—C to...

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Autores principales: Kaewmanee, Narissara, Chantrapromma, Suchada, Boonnak, Nawong, Fun, Hoong-Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685059/
https://www.ncbi.nlm.nih.gov/pubmed/23795078
http://dx.doi.org/10.1107/S1600536813012580
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author Kaewmanee, Narissara
Chantrapromma, Suchada
Boonnak, Nawong
Fun, Hoong-Kun
author_facet Kaewmanee, Narissara
Chantrapromma, Suchada
Boonnak, Nawong
Fun, Hoong-Kun
author_sort Kaewmanee, Narissara
collection PubMed
description The mol­ecule of the title compound, C(15)H(15)NO(2), adopts a trans conformation with respect to the methyl­idene C=N bond and is twisted with a dihedral angle of 26.31 (5)° between the two substituted benzene rings. The eth­oxy group is almost coplanar with the bound benzene ring with a C—O—C—C torsion angle of −179.08 (9)°. In the crystal, mol­ecules are linked by O—H⋯N hydrogen bonds and weak C—H⋯O inter­actions into chains propagating in the [011] and [01-1] directions. C—H⋯π inter­actions are also present.
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spelling pubmed-36850592013-06-21 4-[(E)-(4-Eth­oxy­benzyl­idene)amino]­phenol Kaewmanee, Narissara Chantrapromma, Suchada Boonnak, Nawong Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers The mol­ecule of the title compound, C(15)H(15)NO(2), adopts a trans conformation with respect to the methyl­idene C=N bond and is twisted with a dihedral angle of 26.31 (5)° between the two substituted benzene rings. The eth­oxy group is almost coplanar with the bound benzene ring with a C—O—C—C torsion angle of −179.08 (9)°. In the crystal, mol­ecules are linked by O—H⋯N hydrogen bonds and weak C—H⋯O inter­actions into chains propagating in the [011] and [01-1] directions. C—H⋯π inter­actions are also present. International Union of Crystallography 2013-05-18 /pmc/articles/PMC3685059/ /pubmed/23795078 http://dx.doi.org/10.1107/S1600536813012580 Text en © Kaewmanee et al. 2013 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
Kaewmanee, Narissara
Chantrapromma, Suchada
Boonnak, Nawong
Fun, Hoong-Kun
4-[(E)-(4-Eth­oxy­benzyl­idene)amino]­phenol
title 4-[(E)-(4-Eth­oxy­benzyl­idene)amino]­phenol
title_full 4-[(E)-(4-Eth­oxy­benzyl­idene)amino]­phenol
title_fullStr 4-[(E)-(4-Eth­oxy­benzyl­idene)amino]­phenol
title_full_unstemmed 4-[(E)-(4-Eth­oxy­benzyl­idene)amino]­phenol
title_short 4-[(E)-(4-Eth­oxy­benzyl­idene)amino]­phenol
title_sort 4-[(e)-(4-eth­oxy­benzyl­idene)amino]­phenol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685059/
https://www.ncbi.nlm.nih.gov/pubmed/23795078
http://dx.doi.org/10.1107/S1600536813012580
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AT chantraprommasuchada 4e4ethoxybenzylideneaminophenol
AT boonnaknawong 4e4ethoxybenzylideneaminophenol
AT funhoongkun 4e4ethoxybenzylideneaminophenol

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