(2E)-1-(2-Hy­droxy-5-methyl­phen­yl)-3-(4-meth­oxy­phen­yl)prop-2-en-1-one

In the title compound, C(17)H(16)O(3), the dihedral angle between the aromatic rings is 4.59 (7)° and an intra­molecular O—H⋯O hydrogen bond generates an S(6) ring. In the crystal, adjacent mol­ecules are linked by C—H⋯O hydrogen bonds, leading to the formation of [001] supra­molecular chains. Weak...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Arshad, Suhana, Sarojini, B. K., Khaleel, V. Musthafa, Narayana, B.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089145/
https://www.ncbi.nlm.nih.gov/pubmed/21754540
http://dx.doi.org/10.1107/S1600536811015054
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author Fun, Hoong-Kun
Arshad, Suhana
Sarojini, B. K.
Khaleel, V. Musthafa
Narayana, B.
author_facet Fun, Hoong-Kun
Arshad, Suhana
Sarojini, B. K.
Khaleel, V. Musthafa
Narayana, B.
author_sort Fun, Hoong-Kun
collection PubMed
description In the title compound, C(17)H(16)O(3), the dihedral angle between the aromatic rings is 4.59 (7)° and an intra­molecular O—H⋯O hydrogen bond generates an S(6) ring. In the crystal, adjacent mol­ecules are linked by C—H⋯O hydrogen bonds, leading to the formation of [001] supra­molecular chains. Weak C—H⋯π inter­actions consolidate the packing.
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spelling pubmed-30891452011-07-13 (2E)-1-(2-Hy­droxy-5-methyl­phen­yl)-3-(4-meth­oxy­phen­yl)prop-2-en-1-one Fun, Hoong-Kun Arshad, Suhana Sarojini, B. K. Khaleel, V. Musthafa Narayana, B. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(17)H(16)O(3), the dihedral angle between the aromatic rings is 4.59 (7)° and an intra­molecular O—H⋯O hydrogen bond generates an S(6) ring. In the crystal, adjacent mol­ecules are linked by C—H⋯O hydrogen bonds, leading to the formation of [001] supra­molecular chains. Weak C—H⋯π inter­actions consolidate the packing. International Union of Crystallography 2011-04-29 /pmc/articles/PMC3089145/ /pubmed/21754540 http://dx.doi.org/10.1107/S1600536811015054 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
Arshad, Suhana
Sarojini, B. K.
Khaleel, V. Musthafa
Narayana, B.
(2E)-1-(2-Hy­droxy-5-methyl­phen­yl)-3-(4-meth­oxy­phen­yl)prop-2-en-1-one
title (2E)-1-(2-Hy­droxy-5-methyl­phen­yl)-3-(4-meth­oxy­phen­yl)prop-2-en-1-one
title_full (2E)-1-(2-Hy­droxy-5-methyl­phen­yl)-3-(4-meth­oxy­phen­yl)prop-2-en-1-one
title_fullStr (2E)-1-(2-Hy­droxy-5-methyl­phen­yl)-3-(4-meth­oxy­phen­yl)prop-2-en-1-one
title_full_unstemmed (2E)-1-(2-Hy­droxy-5-methyl­phen­yl)-3-(4-meth­oxy­phen­yl)prop-2-en-1-one
title_short (2E)-1-(2-Hy­droxy-5-methyl­phen­yl)-3-(4-meth­oxy­phen­yl)prop-2-en-1-one
title_sort (2e)-1-(2-hy­droxy-5-methyl­phen­yl)-3-(4-meth­oxy­phen­yl)prop-2-en-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089145/
https://www.ncbi.nlm.nih.gov/pubmed/21754540
http://dx.doi.org/10.1107/S1600536811015054
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