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4,4,4-Trifluoro-3-hy­droxy-3-(trifluoro­meth­yl)butanoic acid

The asymmetric unit of the title compound, C(5)H(4)F(6)O(3), a polyfluorinated derivative of β-hy­droxy­butyric acid, comprises two mol­ecules. Intra­molecular O—H⋯O hydrogen bonds occur. In the crystal, inter­molecular O—H⋯O hydrogen bonds give rise to the formation of carb­oxy­lic acid dimers. Alo...

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Detalles Bibliográficos
Autores principales: Betz, Richard, Gerber, Thomas, Schalekamp, Henk
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051966/
https://www.ncbi.nlm.nih.gov/pubmed/21522373
http://dx.doi.org/10.1107/S1600536811004764
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author Betz, Richard
Gerber, Thomas
Schalekamp, Henk
author_facet Betz, Richard
Gerber, Thomas
Schalekamp, Henk
author_sort Betz, Richard
collection PubMed
description The asymmetric unit of the title compound, C(5)H(4)F(6)O(3), a polyfluorinated derivative of β-hy­droxy­butyric acid, comprises two mol­ecules. Intra­molecular O—H⋯O hydrogen bonds occur. In the crystal, inter­molecular O—H⋯O hydrogen bonds give rise to the formation of carb­oxy­lic acid dimers. Along with these hydrogen bonds, C—H⋯O contacts connect the mol­ecules into infinite strands along the a axis.
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spelling pubmed-30519662011-04-26 4,4,4-Trifluoro-3-hy­droxy-3-(trifluoro­meth­yl)butanoic acid Betz, Richard Gerber, Thomas Schalekamp, Henk Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(5)H(4)F(6)O(3), a polyfluorinated derivative of β-hy­droxy­butyric acid, comprises two mol­ecules. Intra­molecular O—H⋯O hydrogen bonds occur. In the crystal, inter­molecular O—H⋯O hydrogen bonds give rise to the formation of carb­oxy­lic acid dimers. Along with these hydrogen bonds, C—H⋯O contacts connect the mol­ecules into infinite strands along the a axis. International Union of Crystallography 2011-02-12 /pmc/articles/PMC3051966/ /pubmed/21522373 http://dx.doi.org/10.1107/S1600536811004764 Text en © Betz 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
Betz, Richard
Gerber, Thomas
Schalekamp, Henk
4,4,4-Trifluoro-3-hy­droxy-3-(trifluoro­meth­yl)butanoic acid
title 4,4,4-Trifluoro-3-hy­droxy-3-(trifluoro­meth­yl)butanoic acid
title_full 4,4,4-Trifluoro-3-hy­droxy-3-(trifluoro­meth­yl)butanoic acid
title_fullStr 4,4,4-Trifluoro-3-hy­droxy-3-(trifluoro­meth­yl)butanoic acid
title_full_unstemmed 4,4,4-Trifluoro-3-hy­droxy-3-(trifluoro­meth­yl)butanoic acid
title_short 4,4,4-Trifluoro-3-hy­droxy-3-(trifluoro­meth­yl)butanoic acid
title_sort 4,4,4-trifluoro-3-hy­droxy-3-(trifluoro­meth­yl)butanoic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051966/
https://www.ncbi.nlm.nih.gov/pubmed/21522373
http://dx.doi.org/10.1107/S1600536811004764
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