(E)-3-(3,5-Dimeth­oxy­phen­yl)-1-(1-hy­droxy­naphthalen-2-yl)prop-2-en-1-one

In the title mol­ecule, C(21)H(18)O(4), the C=C bond of the central enone group adopts a trans conformation. The dihedral angle formed by the naphthalene ring system and the benzene ring is 2.97 (11)°. The hy­droxy group is involved in an intra­molecular O—H⋯O hydrogen bond. In the crystal, weak C—H...

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Detalles Bibliográficos
Autores principales: Lee, Ha-Jin, Lim, Yoongho, Koh, Dongsoo
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/PMC3588993/
https://www.ncbi.nlm.nih.gov/pubmed/23476229
http://dx.doi.org/10.1107/S1600536812046715
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author Lee, Ha-Jin
Lim, Yoongho
Koh, Dongsoo
author_facet Lee, Ha-Jin
Lim, Yoongho
Koh, Dongsoo
author_sort Lee, Ha-Jin
collection PubMed
description In the title mol­ecule, C(21)H(18)O(4), the C=C bond of the central enone group adopts a trans conformation. The dihedral angle formed by the naphthalene ring system and the benzene ring is 2.97 (11)°. The hy­droxy group is involved in an intra­molecular O—H⋯O hydrogen bond. In the crystal, weak C—H⋯O hydrogen bonds link the mol­ecules into chains along [001].
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spelling pubmed-35889932013-03-08 (E)-3-(3,5-Dimeth­oxy­phen­yl)-1-(1-hy­droxy­naphthalen-2-yl)prop-2-en-1-one Lee, Ha-Jin Lim, Yoongho Koh, Dongsoo Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title mol­ecule, C(21)H(18)O(4), the C=C bond of the central enone group adopts a trans conformation. The dihedral angle formed by the naphthalene ring system and the benzene ring is 2.97 (11)°. The hy­droxy group is involved in an intra­molecular O—H⋯O hydrogen bond. In the crystal, weak C—H⋯O hydrogen bonds link the mol­ecules into chains along [001]. International Union of Crystallography 2012-11-24 /pmc/articles/PMC3588993/ /pubmed/23476229 http://dx.doi.org/10.1107/S1600536812046715 Text en © Lee 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
Lee, Ha-Jin
Lim, Yoongho
Koh, Dongsoo
(E)-3-(3,5-Dimeth­oxy­phen­yl)-1-(1-hy­droxy­naphthalen-2-yl)prop-2-en-1-one
title (E)-3-(3,5-Dimeth­oxy­phen­yl)-1-(1-hy­droxy­naphthalen-2-yl)prop-2-en-1-one
title_full (E)-3-(3,5-Dimeth­oxy­phen­yl)-1-(1-hy­droxy­naphthalen-2-yl)prop-2-en-1-one
title_fullStr (E)-3-(3,5-Dimeth­oxy­phen­yl)-1-(1-hy­droxy­naphthalen-2-yl)prop-2-en-1-one
title_full_unstemmed (E)-3-(3,5-Dimeth­oxy­phen­yl)-1-(1-hy­droxy­naphthalen-2-yl)prop-2-en-1-one
title_short (E)-3-(3,5-Dimeth­oxy­phen­yl)-1-(1-hy­droxy­naphthalen-2-yl)prop-2-en-1-one
title_sort (e)-3-(3,5-dimeth­oxy­phen­yl)-1-(1-hy­droxy­naphthalen-2-yl)prop-2-en-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588993/
https://www.ncbi.nlm.nih.gov/pubmed/23476229
http://dx.doi.org/10.1107/S1600536812046715
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