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2-Hy­droxy-6-isopropyl-3-methyl­benzoic acid

The title compound, C(11)H(14)O(3), is a multiple-substituted derivative of benzoic acid. Intra­cyclic C—C—C angles span a range of 117.16 (19)–122.32 (19)°. Apart from intra­molecular hydrogen bonds between hydroxyl and carboxyl groups, inter­molecular hydrogen bonds are present in the crystal stru...

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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/PMC3089340/
https://www.ncbi.nlm.nih.gov/pubmed/21754389
http://dx.doi.org/10.1107/S1600536811011998
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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 title compound, C(11)H(14)O(3), is a multiple-substituted derivative of benzoic acid. Intra­cyclic C—C—C angles span a range of 117.16 (19)–122.32 (19)°. Apart from intra­molecular hydrogen bonds between hydroxyl and carboxyl groups, inter­molecular hydrogen bonds are present in the crystal structure, the latter ones giving rise to centrosymmetric carb­oxy­lic acid dimers.
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spelling pubmed-30893402011-07-13 2-Hy­droxy-6-isopropyl-3-methyl­benzoic acid Betz, Richard Gerber, Thomas Schalekamp, Henk Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(11)H(14)O(3), is a multiple-substituted derivative of benzoic acid. Intra­cyclic C—C—C angles span a range of 117.16 (19)–122.32 (19)°. Apart from intra­molecular hydrogen bonds between hydroxyl and carboxyl groups, inter­molecular hydrogen bonds are present in the crystal structure, the latter ones giving rise to centrosymmetric carb­oxy­lic acid dimers. International Union of Crystallography 2011-04-07 /pmc/articles/PMC3089340/ /pubmed/21754389 http://dx.doi.org/10.1107/S1600536811011998 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
2-Hy­droxy-6-isopropyl-3-methyl­benzoic acid
title 2-Hy­droxy-6-isopropyl-3-methyl­benzoic acid
title_full 2-Hy­droxy-6-isopropyl-3-methyl­benzoic acid
title_fullStr 2-Hy­droxy-6-isopropyl-3-methyl­benzoic acid
title_full_unstemmed 2-Hy­droxy-6-isopropyl-3-methyl­benzoic acid
title_short 2-Hy­droxy-6-isopropyl-3-methyl­benzoic acid
title_sort 2-hy­droxy-6-isopropyl-3-methyl­benzoic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089340/
https://www.ncbi.nlm.nih.gov/pubmed/21754389
http://dx.doi.org/10.1107/S1600536811011998
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AT schalekamphenk 2hydroxy6isopropyl3methylbenzoicacid