Cargando…

(8-Hy­droxy-6-meth­oxy-1-oxo-1H-isochromen-3-yl)methyl formate: a supra­molecular framework

In the title compound, C(12)H(10)O(6), an intra­molecular O—H⋯O hydrogen bond forms an S(6) ring motif. The mol­ecule is essentially planar with an r.m.s. deviation of 0.051 Å for all non-H atoms. In the crystal mol­ecules are linked by C—H⋯O hydrogen bonds and a C—H⋯π inter­action, forming a supra­...

Descripción completa

Detalles Bibliográficos
Autores principales: Tiouabi, Mustapha, Tabacchi, Raphaël, Stoeckli-Evans, Helen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462167/
https://www.ncbi.nlm.nih.gov/pubmed/36339028
http://dx.doi.org/10.1107/S2414314620013917
_version_ 1784787120363143168
author Tiouabi, Mustapha
Tabacchi, Raphaël
Stoeckli-Evans, Helen
author_facet Tiouabi, Mustapha
Tabacchi, Raphaël
Stoeckli-Evans, Helen
author_sort Tiouabi, Mustapha
collection PubMed
description In the title compound, C(12)H(10)O(6), an intra­molecular O—H⋯O hydrogen bond forms an S(6) ring motif. The mol­ecule is essentially planar with an r.m.s. deviation of 0.051 Å for all non-H atoms. In the crystal mol­ecules are linked by C—H⋯O hydrogen bonds and a C—H⋯π inter­action, forming a supra­molecular framework. [Image: see text]
format Online
Article
Text
id pubmed-9462167
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-94621672022-11-04 (8-Hy­droxy-6-meth­oxy-1-oxo-1H-isochromen-3-yl)methyl formate: a supra­molecular framework Tiouabi, Mustapha Tabacchi, Raphaël Stoeckli-Evans, Helen IUCrdata Data Reports In the title compound, C(12)H(10)O(6), an intra­molecular O—H⋯O hydrogen bond forms an S(6) ring motif. The mol­ecule is essentially planar with an r.m.s. deviation of 0.051 Å for all non-H atoms. In the crystal mol­ecules are linked by C—H⋯O hydrogen bonds and a C—H⋯π inter­action, forming a supra­molecular framework. [Image: see text] International Union of Crystallography 2020-10-23 /pmc/articles/PMC9462167/ /pubmed/36339028 http://dx.doi.org/10.1107/S2414314620013917 Text en © Tiouabi et al. 2020 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Data Reports
Tiouabi, Mustapha
Tabacchi, Raphaël
Stoeckli-Evans, Helen
(8-Hy­droxy-6-meth­oxy-1-oxo-1H-isochromen-3-yl)methyl formate: a supra­molecular framework
title (8-Hy­droxy-6-meth­oxy-1-oxo-1H-isochromen-3-yl)methyl formate: a supra­molecular framework
title_full (8-Hy­droxy-6-meth­oxy-1-oxo-1H-isochromen-3-yl)methyl formate: a supra­molecular framework
title_fullStr (8-Hy­droxy-6-meth­oxy-1-oxo-1H-isochromen-3-yl)methyl formate: a supra­molecular framework
title_full_unstemmed (8-Hy­droxy-6-meth­oxy-1-oxo-1H-isochromen-3-yl)methyl formate: a supra­molecular framework
title_short (8-Hy­droxy-6-meth­oxy-1-oxo-1H-isochromen-3-yl)methyl formate: a supra­molecular framework
title_sort (8-hy­droxy-6-meth­oxy-1-oxo-1h-isochromen-3-yl)methyl formate: a supra­molecular framework
topic Data Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462167/
https://www.ncbi.nlm.nih.gov/pubmed/36339028
http://dx.doi.org/10.1107/S2414314620013917
work_keys_str_mv AT tiouabimustapha 8hydroxy6methoxy1oxo1hisochromen3ylmethylformateasupramolecularframework
AT tabacchiraphael 8hydroxy6methoxy1oxo1hisochromen3ylmethylformateasupramolecularframework
AT stoecklievanshelen 8hydroxy6methoxy1oxo1hisochromen3ylmethylformateasupramolecularframework