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Dimethyl 2,6-dihydroxybenzene-1,4-dicarboxylate
The title compound, C(10)H(10)O(6), was obtained from an esterification reaction of 2,6-dihydroxyterephthalic acid and methanol. In the molecular structure, all of the C atoms are nearly coplanar. The two hydroxy groups have C2 symmetry. Intramolecular O—H⋯O hydrogen bonds are observed. In the c...
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983891/ https://www.ncbi.nlm.nih.gov/pubmed/21580778 http://dx.doi.org/10.1107/S1600536810011074 |
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author | Zhao, Deming Wang, Kun Zhang, Jianting Jin, Ningren |
author_facet | Zhao, Deming Wang, Kun Zhang, Jianting Jin, Ningren |
author_sort | Zhao, Deming |
collection | PubMed |
description | The title compound, C(10)H(10)O(6), was obtained from an esterification reaction of 2,6-dihydroxyterephthalic acid and methanol. In the molecular structure, all of the C atoms are nearly coplanar. The two hydroxy groups have C2 symmetry. Intramolecular O—H⋯O hydrogen bonds are observed. In the crystal, weak O—H⋯O interactions link the molecules. |
format | Text |
id | pubmed-2983891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29838912010-12-30 Dimethyl 2,6-dihydroxybenzene-1,4-dicarboxylate Zhao, Deming Wang, Kun Zhang, Jianting Jin, Ningren Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(10)H(10)O(6), was obtained from an esterification reaction of 2,6-dihydroxyterephthalic acid and methanol. In the molecular structure, all of the C atoms are nearly coplanar. The two hydroxy groups have C2 symmetry. Intramolecular O—H⋯O hydrogen bonds are observed. In the crystal, weak O—H⋯O interactions link the molecules. International Union of Crystallography 2010-03-31 /pmc/articles/PMC2983891/ /pubmed/21580778 http://dx.doi.org/10.1107/S1600536810011074 Text en © Zhao et al. 2010 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 Zhao, Deming Wang, Kun Zhang, Jianting Jin, Ningren Dimethyl 2,6-dihydroxybenzene-1,4-dicarboxylate |
title | Dimethyl 2,6-dihydroxybenzene-1,4-dicarboxylate |
title_full | Dimethyl 2,6-dihydroxybenzene-1,4-dicarboxylate |
title_fullStr | Dimethyl 2,6-dihydroxybenzene-1,4-dicarboxylate |
title_full_unstemmed | Dimethyl 2,6-dihydroxybenzene-1,4-dicarboxylate |
title_short | Dimethyl 2,6-dihydroxybenzene-1,4-dicarboxylate |
title_sort | dimethyl 2,6-dihydroxybenzene-1,4-dicarboxylate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983891/ https://www.ncbi.nlm.nih.gov/pubmed/21580778 http://dx.doi.org/10.1107/S1600536810011074 |
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