Methyl 3,5-bis­[(4-hydroxy­methyl-2-methoxy­phen­oxy)meth­yl]benzoate

In the title compound, C(26)H(28)O(8), the central aromatic ring forms dihedral angles of 24.32 (11) and 80.19 (7)° with the two adjoining vanillyl alcohol rings. In the crystal, O—H⋯O hydrogen bonds connect the mol­ecules, forming a hydrogen-bonded sheet-like motif extended in the ab plane....

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Detalles Bibliográficos
Autores principales: Arshad, Muhammad Nadeem, Mough, Scott T., Goeltz, John C., Holman, K. Travis
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983507/
https://www.ncbi.nlm.nih.gov/pubmed/21580441
http://dx.doi.org/10.1107/S160053681000677X
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author Arshad, Muhammad Nadeem
Mough, Scott T.
Goeltz, John C.
Holman, K. Travis
author_facet Arshad, Muhammad Nadeem
Mough, Scott T.
Goeltz, John C.
Holman, K. Travis
author_sort Arshad, Muhammad Nadeem
collection PubMed
description In the title compound, C(26)H(28)O(8), the central aromatic ring forms dihedral angles of 24.32 (11) and 80.19 (7)° with the two adjoining vanillyl alcohol rings. In the crystal, O—H⋯O hydrogen bonds connect the mol­ecules, forming a hydrogen-bonded sheet-like motif extended in the ab plane.
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spelling pubmed-29835072010-12-30 Methyl 3,5-bis­[(4-hydroxy­methyl-2-methoxy­phen­oxy)meth­yl]benzoate Arshad, Muhammad Nadeem Mough, Scott T. Goeltz, John C. Holman, K. Travis Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(26)H(28)O(8), the central aromatic ring forms dihedral angles of 24.32 (11) and 80.19 (7)° with the two adjoining vanillyl alcohol rings. In the crystal, O—H⋯O hydrogen bonds connect the mol­ecules, forming a hydrogen-bonded sheet-like motif extended in the ab plane. International Union of Crystallography 2010-02-27 /pmc/articles/PMC2983507/ /pubmed/21580441 http://dx.doi.org/10.1107/S160053681000677X Text en © Arshad 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
Arshad, Muhammad Nadeem
Mough, Scott T.
Goeltz, John C.
Holman, K. Travis
Methyl 3,5-bis­[(4-hydroxy­methyl-2-methoxy­phen­oxy)meth­yl]benzoate
title Methyl 3,5-bis­[(4-hydroxy­methyl-2-methoxy­phen­oxy)meth­yl]benzoate
title_full Methyl 3,5-bis­[(4-hydroxy­methyl-2-methoxy­phen­oxy)meth­yl]benzoate
title_fullStr Methyl 3,5-bis­[(4-hydroxy­methyl-2-methoxy­phen­oxy)meth­yl]benzoate
title_full_unstemmed Methyl 3,5-bis­[(4-hydroxy­methyl-2-methoxy­phen­oxy)meth­yl]benzoate
title_short Methyl 3,5-bis­[(4-hydroxy­methyl-2-methoxy­phen­oxy)meth­yl]benzoate
title_sort methyl 3,5-bis­[(4-hydroxy­methyl-2-methoxy­phen­oxy)meth­yl]benzoate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983507/
https://www.ncbi.nlm.nih.gov/pubmed/21580441
http://dx.doi.org/10.1107/S160053681000677X
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