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(E)-1-[4-(Hex­yloxy)phen­yl]-3-(4-hy­droxy­phen­yl)prop-2-en-1-one

In the title compound, C(21)H(24)O(3), inter­molecular O—H⋯O and C—H⋯O inter­actions form bifurcated acceptor bonds, generating R (2) (1)(6) ring motifs. These ring motifs link the mol­ecules into extended chains along [010]. The crystal structure is further stabilized by C—H⋯π inter­actions....

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Detalles Bibliográficos
Autores principales: Ngaini, Zainab, Fadzillah, Siti Muhaini Haris, Hussain, Hasnain, Razak, Ibrahim Abdul, Fun, Hoong-Kun
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050273/
https://www.ncbi.nlm.nih.gov/pubmed/21522676
http://dx.doi.org/10.1107/S1600536810052086
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author Ngaini, Zainab
Fadzillah, Siti Muhaini Haris
Hussain, Hasnain
Razak, Ibrahim Abdul
Fun, Hoong-Kun
author_facet Ngaini, Zainab
Fadzillah, Siti Muhaini Haris
Hussain, Hasnain
Razak, Ibrahim Abdul
Fun, Hoong-Kun
author_sort Ngaini, Zainab
collection PubMed
description In the title compound, C(21)H(24)O(3), inter­molecular O—H⋯O and C—H⋯O inter­actions form bifurcated acceptor bonds, generating R (2) (1)(6) ring motifs. These ring motifs link the mol­ecules into extended chains along [010]. The crystal structure is further stabilized by C—H⋯π inter­actions.
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spelling pubmed-30502732011-04-26 (E)-1-[4-(Hex­yloxy)phen­yl]-3-(4-hy­droxy­phen­yl)prop-2-en-1-one Ngaini, Zainab Fadzillah, Siti Muhaini Haris Hussain, Hasnain Razak, Ibrahim Abdul Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(21)H(24)O(3), inter­molecular O—H⋯O and C—H⋯O inter­actions form bifurcated acceptor bonds, generating R (2) (1)(6) ring motifs. These ring motifs link the mol­ecules into extended chains along [010]. The crystal structure is further stabilized by C—H⋯π inter­actions. International Union of Crystallography 2010-12-18 /pmc/articles/PMC3050273/ /pubmed/21522676 http://dx.doi.org/10.1107/S1600536810052086 Text en © Ngaini 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
Ngaini, Zainab
Fadzillah, Siti Muhaini Haris
Hussain, Hasnain
Razak, Ibrahim Abdul
Fun, Hoong-Kun
(E)-1-[4-(Hex­yloxy)phen­yl]-3-(4-hy­droxy­phen­yl)prop-2-en-1-one
title (E)-1-[4-(Hex­yloxy)phen­yl]-3-(4-hy­droxy­phen­yl)prop-2-en-1-one
title_full (E)-1-[4-(Hex­yloxy)phen­yl]-3-(4-hy­droxy­phen­yl)prop-2-en-1-one
title_fullStr (E)-1-[4-(Hex­yloxy)phen­yl]-3-(4-hy­droxy­phen­yl)prop-2-en-1-one
title_full_unstemmed (E)-1-[4-(Hex­yloxy)phen­yl]-3-(4-hy­droxy­phen­yl)prop-2-en-1-one
title_short (E)-1-[4-(Hex­yloxy)phen­yl]-3-(4-hy­droxy­phen­yl)prop-2-en-1-one
title_sort (e)-1-[4-(hex­yloxy)phen­yl]-3-(4-hy­droxy­phen­yl)prop-2-en-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050273/
https://www.ncbi.nlm.nih.gov/pubmed/21522676
http://dx.doi.org/10.1107/S1600536810052086
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