2-(Acet­oxy­meth­yl)benzoic acid

The title compound, C(10)H(10)O(4), crystallizes with the well-known carb­oxy­lic acid dimer-forming R (2) (2)(8) hydrogen-bond motif. Chains approximately parallel to (-1-12) are then built through C(methyl­ene,phen­yl)–H⋯O(carbon­yl) inter­actions [C(6) and C(8) motifs] with one (meth­yl)C—H⋯π int...

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Detalles Bibliográficos
Autores principales: Gainsford, Graeme J., Schwörer, Ralf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569790/
https://www.ncbi.nlm.nih.gov/pubmed/23424536
http://dx.doi.org/10.1107/S1600536813000780
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author Gainsford, Graeme J.
Schwörer, Ralf
author_facet Gainsford, Graeme J.
Schwörer, Ralf
author_sort Gainsford, Graeme J.
collection PubMed
description The title compound, C(10)H(10)O(4), crystallizes with the well-known carb­oxy­lic acid dimer-forming R (2) (2)(8) hydrogen-bond motif. Chains approximately parallel to (-1-12) are then built through C(methyl­ene,phen­yl)–H⋯O(carbon­yl) inter­actions [C(6) and C(8) motifs] with one (meth­yl)C—H⋯π inter­action providing inter­planar binding. The weakness of the latter inter­action is consistent with the difficulty experienced in obtaining suitable single crystals.
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spelling pubmed-35697902013-02-19 2-(Acet­oxy­meth­yl)benzoic acid Gainsford, Graeme J. Schwörer, Ralf Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(10)H(10)O(4), crystallizes with the well-known carb­oxy­lic acid dimer-forming R (2) (2)(8) hydrogen-bond motif. Chains approximately parallel to (-1-12) are then built through C(methyl­ene,phen­yl)–H⋯O(carbon­yl) inter­actions [C(6) and C(8) motifs] with one (meth­yl)C—H⋯π inter­action providing inter­planar binding. The weakness of the latter inter­action is consistent with the difficulty experienced in obtaining suitable single crystals. International Union of Crystallography 2013-01-19 /pmc/articles/PMC3569790/ /pubmed/23424536 http://dx.doi.org/10.1107/S1600536813000780 Text en © Gainsford and Schwörer 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
Gainsford, Graeme J.
Schwörer, Ralf
2-(Acet­oxy­meth­yl)benzoic acid
title 2-(Acet­oxy­meth­yl)benzoic acid
title_full 2-(Acet­oxy­meth­yl)benzoic acid
title_fullStr 2-(Acet­oxy­meth­yl)benzoic acid
title_full_unstemmed 2-(Acet­oxy­meth­yl)benzoic acid
title_short 2-(Acet­oxy­meth­yl)benzoic acid
title_sort 2-(acet­oxy­meth­yl)benzoic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569790/
https://www.ncbi.nlm.nih.gov/pubmed/23424536
http://dx.doi.org/10.1107/S1600536813000780
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