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1-(3-Chloro­phen­yl)-5-(2,4-di­hydroxy­benzo­yl)pyridin-2(1H)-one

The chloro­phenyl group of the title compound, C(18)H(12)ClNO(4), is disordered over two orientations with occupancies of 0.331 (8) and 0.669 (8). An intra­molecular hydrogen bond is formed between a hy­droxy group and the acyclic carbonyl group. In the crystal, molecules are linked into chains alon...

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Detalles Bibliográficos
Autores principales: Ren, Fang, Li, Guifeng, Zhang, Quanying, Yao, Jinhua, Zhang, Xuli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648264/
https://www.ncbi.nlm.nih.gov/pubmed/23723884
http://dx.doi.org/10.1107/S1600536813009689
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author Ren, Fang
Li, Guifeng
Zhang, Quanying
Yao, Jinhua
Zhang, Xuli
author_facet Ren, Fang
Li, Guifeng
Zhang, Quanying
Yao, Jinhua
Zhang, Xuli
author_sort Ren, Fang
collection PubMed
description The chloro­phenyl group of the title compound, C(18)H(12)ClNO(4), is disordered over two orientations with occupancies of 0.331 (8) and 0.669 (8). An intra­molecular hydrogen bond is formed between a hy­droxy group and the acyclic carbonyl group. In the crystal, molecules are linked into chains along [110] by O—H⋯O and C—H⋯O hydrogen bonds, forming a ladder motif.
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spelling pubmed-36482642013-05-30 1-(3-Chloro­phen­yl)-5-(2,4-di­hydroxy­benzo­yl)pyridin-2(1H)-one Ren, Fang Li, Guifeng Zhang, Quanying Yao, Jinhua Zhang, Xuli Acta Crystallogr Sect E Struct Rep Online Organic Papers The chloro­phenyl group of the title compound, C(18)H(12)ClNO(4), is disordered over two orientations with occupancies of 0.331 (8) and 0.669 (8). An intra­molecular hydrogen bond is formed between a hy­droxy group and the acyclic carbonyl group. In the crystal, molecules are linked into chains along [110] by O—H⋯O and C—H⋯O hydrogen bonds, forming a ladder motif. International Union of Crystallography 2013-04-13 /pmc/articles/PMC3648264/ /pubmed/23723884 http://dx.doi.org/10.1107/S1600536813009689 Text en © Ren et al. 2013 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
Ren, Fang
Li, Guifeng
Zhang, Quanying
Yao, Jinhua
Zhang, Xuli
1-(3-Chloro­phen­yl)-5-(2,4-di­hydroxy­benzo­yl)pyridin-2(1H)-one
title 1-(3-Chloro­phen­yl)-5-(2,4-di­hydroxy­benzo­yl)pyridin-2(1H)-one
title_full 1-(3-Chloro­phen­yl)-5-(2,4-di­hydroxy­benzo­yl)pyridin-2(1H)-one
title_fullStr 1-(3-Chloro­phen­yl)-5-(2,4-di­hydroxy­benzo­yl)pyridin-2(1H)-one
title_full_unstemmed 1-(3-Chloro­phen­yl)-5-(2,4-di­hydroxy­benzo­yl)pyridin-2(1H)-one
title_short 1-(3-Chloro­phen­yl)-5-(2,4-di­hydroxy­benzo­yl)pyridin-2(1H)-one
title_sort 1-(3-chloro­phen­yl)-5-(2,4-di­hydroxy­benzo­yl)pyridin-2(1h)-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648264/
https://www.ncbi.nlm.nih.gov/pubmed/23723884
http://dx.doi.org/10.1107/S1600536813009689
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