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

In the title compound, C(25)H(32)O(3), the enone group is in an s–cis configuration. The dihedral angle between the benzene rings is 8.84 (7)°. An intra­molecular O—H⋯O inter­action between the keto and hydr­oxy groups forms an S(6) ring motif. Inter­molecular C—H⋯O inter­actions link the mol­ecules...

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Detalles Bibliográficos
Autores principales: Ngaini, Zainab, Rahman, Norashikin Irdawaty Abd, Hussain, Hasnain, Razak, Ibrahim Abdul, Fun, Hoong-Kun
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968804/
https://www.ncbi.nlm.nih.gov/pubmed/21582598
http://dx.doi.org/10.1107/S1600536809010848
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author Ngaini, Zainab
Rahman, Norashikin Irdawaty Abd
Hussain, Hasnain
Razak, Ibrahim Abdul
Fun, Hoong-Kun
author_facet Ngaini, Zainab
Rahman, Norashikin Irdawaty Abd
Hussain, Hasnain
Razak, Ibrahim Abdul
Fun, Hoong-Kun
author_sort Ngaini, Zainab
collection PubMed
description In the title compound, C(25)H(32)O(3), the enone group is in an s–cis configuration. The dihedral angle between the benzene rings is 8.84 (7)°. An intra­molecular O—H⋯O inter­action between the keto and hydr­oxy groups forms an S(6) ring motif. Inter­molecular C—H⋯O inter­actions link the mol­ecules into supra­molecular chains along the c axis which are subsequently stacked down the b axis; the crystal structure is further consolidated by C—H⋯π inter­actions.
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spelling pubmed-29688042010-12-30 (E)-3-(4-Decyl­oxyphen­yl)-1-(2-hydroxy­phen­yl)prop-2-en-1-one Ngaini, Zainab Rahman, Norashikin Irdawaty Abd Hussain, Hasnain Razak, Ibrahim Abdul Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(25)H(32)O(3), the enone group is in an s–cis configuration. The dihedral angle between the benzene rings is 8.84 (7)°. An intra­molecular O—H⋯O inter­action between the keto and hydr­oxy groups forms an S(6) ring motif. Inter­molecular C—H⋯O inter­actions link the mol­ecules into supra­molecular chains along the c axis which are subsequently stacked down the b axis; the crystal structure is further consolidated by C—H⋯π inter­actions. International Union of Crystallography 2009-03-28 /pmc/articles/PMC2968804/ /pubmed/21582598 http://dx.doi.org/10.1107/S1600536809010848 Text en © Ngaini 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
Ngaini, Zainab
Rahman, Norashikin Irdawaty Abd
Hussain, Hasnain
Razak, Ibrahim Abdul
Fun, Hoong-Kun
(E)-3-(4-Decyl­oxyphen­yl)-1-(2-hydroxy­phen­yl)prop-2-en-1-one
title (E)-3-(4-Decyl­oxyphen­yl)-1-(2-hydroxy­phen­yl)prop-2-en-1-one
title_full (E)-3-(4-Decyl­oxyphen­yl)-1-(2-hydroxy­phen­yl)prop-2-en-1-one
title_fullStr (E)-3-(4-Decyl­oxyphen­yl)-1-(2-hydroxy­phen­yl)prop-2-en-1-one
title_full_unstemmed (E)-3-(4-Decyl­oxyphen­yl)-1-(2-hydroxy­phen­yl)prop-2-en-1-one
title_short (E)-3-(4-Decyl­oxyphen­yl)-1-(2-hydroxy­phen­yl)prop-2-en-1-one
title_sort (e)-3-(4-decyl­oxyphen­yl)-1-(2-hydroxy­phen­yl)prop-2-en-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968804/
https://www.ncbi.nlm.nih.gov/pubmed/21582598
http://dx.doi.org/10.1107/S1600536809010848
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