1-(2-Hy­droxy-3,5-dimeth­oxy­phen­yl)ethanone

In title compound, C(10)H(12)O(4), all of the non-H atoms lie approximately in a plane with the largest deviation being 0.061 (2) Å. An intra­molecular O—H⋯O hydrogen bond generates an S(6) ring motif. No classical inter­molecular hydrogen bonding occurs, with only van der Waals forces stabilizing t...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Wenming, Li, Xiaobo, Duan, Yuqing, Deng, Zhirong, Wang, Runling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3254463/
https://www.ncbi.nlm.nih.gov/pubmed/22259403
http://dx.doi.org/10.1107/S1600536811052974
_version_ 1782220859931361280
author Li, Wenming
Li, Xiaobo
Duan, Yuqing
Deng, Zhirong
Wang, Runling
author_facet Li, Wenming
Li, Xiaobo
Duan, Yuqing
Deng, Zhirong
Wang, Runling
author_sort Li, Wenming
collection PubMed
description In title compound, C(10)H(12)O(4), all of the non-H atoms lie approximately in a plane with the largest deviation being 0.061 (2) Å. An intra­molecular O—H⋯O hydrogen bond generates an S(6) ring motif. No classical inter­molecular hydrogen bonding occurs, with only van der Waals forces stabilizing the crystal structure.
format Online
Article
Text
id pubmed-3254463
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-32544632012-01-18 1-(2-Hy­droxy-3,5-dimeth­oxy­phen­yl)ethanone Li, Wenming Li, Xiaobo Duan, Yuqing Deng, Zhirong Wang, Runling Acta Crystallogr Sect E Struct Rep Online Organic Papers In title compound, C(10)H(12)O(4), all of the non-H atoms lie approximately in a plane with the largest deviation being 0.061 (2) Å. An intra­molecular O—H⋯O hydrogen bond generates an S(6) ring motif. No classical inter­molecular hydrogen bonding occurs, with only van der Waals forces stabilizing the crystal structure. International Union of Crystallography 2011-12-14 /pmc/articles/PMC3254463/ /pubmed/22259403 http://dx.doi.org/10.1107/S1600536811052974 Text en © Li et al. 2012 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
Li, Wenming
Li, Xiaobo
Duan, Yuqing
Deng, Zhirong
Wang, Runling
1-(2-Hy­droxy-3,5-dimeth­oxy­phen­yl)ethanone
title 1-(2-Hy­droxy-3,5-dimeth­oxy­phen­yl)ethanone
title_full 1-(2-Hy­droxy-3,5-dimeth­oxy­phen­yl)ethanone
title_fullStr 1-(2-Hy­droxy-3,5-dimeth­oxy­phen­yl)ethanone
title_full_unstemmed 1-(2-Hy­droxy-3,5-dimeth­oxy­phen­yl)ethanone
title_short 1-(2-Hy­droxy-3,5-dimeth­oxy­phen­yl)ethanone
title_sort 1-(2-hy­droxy-3,5-dimeth­oxy­phen­yl)ethanone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3254463/
https://www.ncbi.nlm.nih.gov/pubmed/22259403
http://dx.doi.org/10.1107/S1600536811052974
work_keys_str_mv AT liwenming 12hydroxy35dimethoxyphenylethanone
AT lixiaobo 12hydroxy35dimethoxyphenylethanone
AT duanyuqing 12hydroxy35dimethoxyphenylethanone
AT dengzhirong 12hydroxy35dimethoxyphenylethanone
AT wangrunling 12hydroxy35dimethoxyphenylethanone

Ejemplares similares