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1-(5-Acetyl-2-hy­droxy­phen­yl)ethanone

The crystal structure of the title compound, C(10)H(10)O(3), is characterized by classical intra­molecular hydrogen bonding. The hy­droxy group is disordered over two positions (77 and 23%). The crystal structure is stabilized via π–π [3.5986 (1) Å] and weak nonclassical C—H⋯O inter­actions [3.2797 ...

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Autores principales: Hübscher, Jörg, Izotova, Lidiya, Talipov, Samat, Eissmann, Frank, Weber, Edwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3151842/
https://www.ncbi.nlm.nih.gov/pubmed/21837028
http://dx.doi.org/10.1107/S1600536811020423
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author Hübscher, Jörg
Izotova, Lidiya
Talipov, Samat
Eissmann, Frank
Weber, Edwin
author_facet Hübscher, Jörg
Izotova, Lidiya
Talipov, Samat
Eissmann, Frank
Weber, Edwin
author_sort Hübscher, Jörg
collection PubMed
description The crystal structure of the title compound, C(10)H(10)O(3), is characterized by classical intra­molecular hydrogen bonding. The hy­droxy group is disordered over two positions (77 and 23%). The crystal structure is stabilized via π–π [3.5986 (1) Å] and weak nonclassical C—H⋯O inter­actions [3.2797 (15) Å].
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spelling pubmed-31518422011-08-11 1-(5-Acetyl-2-hy­droxy­phen­yl)ethanone Hübscher, Jörg Izotova, Lidiya Talipov, Samat Eissmann, Frank Weber, Edwin Acta Crystallogr Sect E Struct Rep Online Organic Papers The crystal structure of the title compound, C(10)H(10)O(3), is characterized by classical intra­molecular hydrogen bonding. The hy­droxy group is disordered over two positions (77 and 23%). The crystal structure is stabilized via π–π [3.5986 (1) Å] and weak nonclassical C—H⋯O inter­actions [3.2797 (15) Å]. International Union of Crystallography 2011-06-11 /pmc/articles/PMC3151842/ /pubmed/21837028 http://dx.doi.org/10.1107/S1600536811020423 Text en © Hübscher 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
Hübscher, Jörg
Izotova, Lidiya
Talipov, Samat
Eissmann, Frank
Weber, Edwin
1-(5-Acetyl-2-hy­droxy­phen­yl)ethanone
title 1-(5-Acetyl-2-hy­droxy­phen­yl)ethanone
title_full 1-(5-Acetyl-2-hy­droxy­phen­yl)ethanone
title_fullStr 1-(5-Acetyl-2-hy­droxy­phen­yl)ethanone
title_full_unstemmed 1-(5-Acetyl-2-hy­droxy­phen­yl)ethanone
title_short 1-(5-Acetyl-2-hy­droxy­phen­yl)ethanone
title_sort 1-(5-acetyl-2-hy­droxy­phen­yl)ethanone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3151842/
https://www.ncbi.nlm.nih.gov/pubmed/21837028
http://dx.doi.org/10.1107/S1600536811020423
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