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(E)-1-(4-Decyl­oxyphen­yl)-3-(4-hydroxy­phen­yl)prop-2-en-1-one

In the title compound, C(25)H(32)O(3), the asymmetric unit contains two crystallographically independent mol­ecules: both enone groups adopt an s-cis configuration. In the crystal, O—H⋯O and C—H⋯O inter­molecular inter­actions form bifurcated hydrogen bonds, which generate R (1) (2)(6) ring motifs....

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Detalles Bibliográficos
Autores principales: Razak, Ibrahim Abdul, Fun, Hoong-Kun, Ngaini, Zainab, Fadzillah, Siti Muhaini Haris, Hussain, Hasnain
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969075/
https://www.ncbi.nlm.nih.gov/pubmed/21582591
http://dx.doi.org/10.1107/S160053680901054X
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author Razak, Ibrahim Abdul
Fun, Hoong-Kun
Ngaini, Zainab
Fadzillah, Siti Muhaini Haris
Hussain, Hasnain
author_facet Razak, Ibrahim Abdul
Fun, Hoong-Kun
Ngaini, Zainab
Fadzillah, Siti Muhaini Haris
Hussain, Hasnain
author_sort Razak, Ibrahim Abdul
collection PubMed
description In the title compound, C(25)H(32)O(3), the asymmetric unit contains two crystallographically independent mol­ecules: both enone groups adopt an s-cis configuration. In the crystal, O—H⋯O and C—H⋯O inter­molecular inter­actions form bifurcated hydrogen bonds, which generate R (1) (2)(6) ring motifs. These inter­molecular inter­actions link the mol­ecules into one-dimensional chains along the [10[Image: see text]] direction. The crystal structure is further stabilized by C—H⋯π inter­actions.
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spelling pubmed-29690752010-12-30 (E)-1-(4-Decyl­oxyphen­yl)-3-(4-hydroxy­phen­yl)prop-2-en-1-one Razak, Ibrahim Abdul Fun, Hoong-Kun Ngaini, Zainab Fadzillah, Siti Muhaini Haris Hussain, Hasnain Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(25)H(32)O(3), the asymmetric unit contains two crystallographically independent mol­ecules: both enone groups adopt an s-cis configuration. In the crystal, O—H⋯O and C—H⋯O inter­molecular inter­actions form bifurcated hydrogen bonds, which generate R (1) (2)(6) ring motifs. These inter­molecular inter­actions link the mol­ecules into one-dimensional chains along the [10[Image: see text]] direction. The crystal structure is further stabilized by C—H⋯π inter­actions. International Union of Crystallography 2009-03-28 /pmc/articles/PMC2969075/ /pubmed/21582591 http://dx.doi.org/10.1107/S160053680901054X Text en © Razak et al. 2009 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
Razak, Ibrahim Abdul
Fun, Hoong-Kun
Ngaini, Zainab
Fadzillah, Siti Muhaini Haris
Hussain, Hasnain
(E)-1-(4-Decyl­oxyphen­yl)-3-(4-hydroxy­phen­yl)prop-2-en-1-one
title (E)-1-(4-Decyl­oxyphen­yl)-3-(4-hydroxy­phen­yl)prop-2-en-1-one
title_full (E)-1-(4-Decyl­oxyphen­yl)-3-(4-hydroxy­phen­yl)prop-2-en-1-one
title_fullStr (E)-1-(4-Decyl­oxyphen­yl)-3-(4-hydroxy­phen­yl)prop-2-en-1-one
title_full_unstemmed (E)-1-(4-Decyl­oxyphen­yl)-3-(4-hydroxy­phen­yl)prop-2-en-1-one
title_short (E)-1-(4-Decyl­oxyphen­yl)-3-(4-hydroxy­phen­yl)prop-2-en-1-one
title_sort (e)-1-(4-decyl­oxyphen­yl)-3-(4-hydroxy­phen­yl)prop-2-en-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969075/
https://www.ncbi.nlm.nih.gov/pubmed/21582591
http://dx.doi.org/10.1107/S160053680901054X
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