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1-(5-Chloro-2,4-dihydroxyphenyl)-2-(4-ethoxyphenyl)ethanone
The structure of the title compound, C(16)H(15)ClO(4), contains aryl rings which are inclined by 75.6 (1)° to each other. It displays intramolecular O—H⋯O hydrogen bonding between the 2-hydroxy and carbonyl groups, forming a six-membered ring. Furthermore, the 4-hydroxy group, acting as a hydroge...
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959265/ https://www.ncbi.nlm.nih.gov/pubmed/21201224 http://dx.doi.org/10.1107/S1600536808030699 |
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author | Botting, Nigel P. Slawin, Alexandra M. Z. Zhang, Qingzhi |
author_facet | Botting, Nigel P. Slawin, Alexandra M. Z. Zhang, Qingzhi |
author_sort | Botting, Nigel P. |
collection | PubMed |
description | The structure of the title compound, C(16)H(15)ClO(4), contains aryl rings which are inclined by 75.6 (1)° to each other. It displays intramolecular O—H⋯O hydrogen bonding between the 2-hydroxy and carbonyl groups, forming a six-membered ring. Furthermore, the 4-hydroxy group, acting as a hydrogen-bond donor, is bound to the O atom of the 2-hydroxy group of another molecule. |
format | Text |
id | pubmed-2959265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29592652010-12-30 1-(5-Chloro-2,4-dihydroxyphenyl)-2-(4-ethoxyphenyl)ethanone Botting, Nigel P. Slawin, Alexandra M. Z. Zhang, Qingzhi Acta Crystallogr Sect E Struct Rep Online Organic Papers The structure of the title compound, C(16)H(15)ClO(4), contains aryl rings which are inclined by 75.6 (1)° to each other. It displays intramolecular O—H⋯O hydrogen bonding between the 2-hydroxy and carbonyl groups, forming a six-membered ring. Furthermore, the 4-hydroxy group, acting as a hydrogen-bond donor, is bound to the O atom of the 2-hydroxy group of another molecule. International Union of Crystallography 2008-09-27 /pmc/articles/PMC2959265/ /pubmed/21201224 http://dx.doi.org/10.1107/S1600536808030699 Text en © Botting et al. 2008 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 Botting, Nigel P. Slawin, Alexandra M. Z. Zhang, Qingzhi 1-(5-Chloro-2,4-dihydroxyphenyl)-2-(4-ethoxyphenyl)ethanone |
title | 1-(5-Chloro-2,4-dihydroxyphenyl)-2-(4-ethoxyphenyl)ethanone |
title_full | 1-(5-Chloro-2,4-dihydroxyphenyl)-2-(4-ethoxyphenyl)ethanone |
title_fullStr | 1-(5-Chloro-2,4-dihydroxyphenyl)-2-(4-ethoxyphenyl)ethanone |
title_full_unstemmed | 1-(5-Chloro-2,4-dihydroxyphenyl)-2-(4-ethoxyphenyl)ethanone |
title_short | 1-(5-Chloro-2,4-dihydroxyphenyl)-2-(4-ethoxyphenyl)ethanone |
title_sort | 1-(5-chloro-2,4-dihydroxyphenyl)-2-(4-ethoxyphenyl)ethanone |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959265/ https://www.ncbi.nlm.nih.gov/pubmed/21201224 http://dx.doi.org/10.1107/S1600536808030699 |
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