2-Hy­droxy-N-(2-hy­droxy­eth­yl)benzamide

In the title compound, C(9)H(11)NO(3), a derivative of salicyl­amide, the intra­cyclic C—C—C angles span the range 117.96 (13)–121.56 (14)°. An intra­molecular O—H⋯O hydro­gen bond occurs. In the crystal, inter­molecular O—H⋯O and N—H⋯O hydrogen bonds occur and C—H⋯O contacts connect the mol­ecules...

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Detalles Bibliográficos
Autores principales: Betz, Richard, Gerber, Thomas, Hosten, Eric, Schalekamp, Henk
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/PMC3213558/
https://www.ncbi.nlm.nih.gov/pubmed/22091135
http://dx.doi.org/10.1107/S1600536811029175
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author Betz, Richard
Gerber, Thomas
Hosten, Eric
Schalekamp, Henk
author_facet Betz, Richard
Gerber, Thomas
Hosten, Eric
Schalekamp, Henk
author_sort Betz, Richard
collection PubMed
description In the title compound, C(9)H(11)NO(3), a derivative of salicyl­amide, the intra­cyclic C—C—C angles span the range 117.96 (13)–121.56 (14)°. An intra­molecular O—H⋯O hydro­gen bond occurs. In the crystal, inter­molecular O—H⋯O and N—H⋯O hydrogen bonds occur and C—H⋯O contacts connect the mol­ecules into a three-dimensional network. The closest inter­centroid distance between two π-systems is 3.8809 (10) Å.
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spelling pubmed-32135582011-11-16 2-Hy­droxy-N-(2-hy­droxy­eth­yl)benzamide Betz, Richard Gerber, Thomas Hosten, Eric Schalekamp, Henk Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(9)H(11)NO(3), a derivative of salicyl­amide, the intra­cyclic C—C—C angles span the range 117.96 (13)–121.56 (14)°. An intra­molecular O—H⋯O hydro­gen bond occurs. In the crystal, inter­molecular O—H⋯O and N—H⋯O hydrogen bonds occur and C—H⋯O contacts connect the mol­ecules into a three-dimensional network. The closest inter­centroid distance between two π-systems is 3.8809 (10) Å. International Union of Crystallography 2011-07-23 /pmc/articles/PMC3213558/ /pubmed/22091135 http://dx.doi.org/10.1107/S1600536811029175 Text en © Betz et al. 2011 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
Betz, Richard
Gerber, Thomas
Hosten, Eric
Schalekamp, Henk
2-Hy­droxy-N-(2-hy­droxy­eth­yl)benzamide
title 2-Hy­droxy-N-(2-hy­droxy­eth­yl)benzamide
title_full 2-Hy­droxy-N-(2-hy­droxy­eth­yl)benzamide
title_fullStr 2-Hy­droxy-N-(2-hy­droxy­eth­yl)benzamide
title_full_unstemmed 2-Hy­droxy-N-(2-hy­droxy­eth­yl)benzamide
title_short 2-Hy­droxy-N-(2-hy­droxy­eth­yl)benzamide
title_sort 2-hy­droxy-n-(2-hy­droxy­eth­yl)benzamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213558/
https://www.ncbi.nlm.nih.gov/pubmed/22091135
http://dx.doi.org/10.1107/S1600536811029175
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AT gerberthomas 2hydroxyn2hydroxyethylbenzamide
AT hosteneric 2hydroxyn2hydroxyethylbenzamide
AT schalekamphenk 2hydroxyn2hydroxyethylbenzamide

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