N-(4-Hy­droxy-2-nitro­phen­yl)acetamide

The title compound, C(8)H(8)N(2)O(4), differs in its degree of planarity from the 3-nitro isomer and also in its hydrogen-bonding pattern. Its NH group forms an intra­molecular hydrogen bond to a nitro oxygen atom, and its OH group forms an inter­molecular hydrogen bond to an amide oxygen atom, gene...

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Autores principales: Hines III, James E., Deere, Curtistine J., Fronczek, Frank R., Uppu, Rao M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2022
Materias:
Data Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462003/
https://www.ncbi.nlm.nih.gov/pubmed/36340874
http://dx.doi.org/10.1107/S2414314622002012
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author Hines III, James E.
Deere, Curtistine J.
Fronczek, Frank R.
Uppu, Rao M.
author_facet Hines III, James E.
Deere, Curtistine J.
Fronczek, Frank R.
Uppu, Rao M.
author_sort Hines III, James E.
collection PubMed
description The title compound, C(8)H(8)N(2)O(4), differs in its degree of planarity from the 3-nitro isomer and also in its hydrogen-bonding pattern. Its NH group forms an intra­molecular hydrogen bond to a nitro oxygen atom, and its OH group forms an inter­molecular hydrogen bond to an amide oxygen atom, generating [10 [Image: see text] ] chains in the crystal. [Image: see text]
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spelling pubmed-94620032022-11-04 N-(4-Hy­droxy-2-nitro­phen­yl)acetamide Hines III, James E. Deere, Curtistine J. Fronczek, Frank R. Uppu, Rao M. IUCrdata Data Reports The title compound, C(8)H(8)N(2)O(4), differs in its degree of planarity from the 3-nitro isomer and also in its hydrogen-bonding pattern. Its NH group forms an intra­molecular hydrogen bond to a nitro oxygen atom, and its OH group forms an inter­molecular hydrogen bond to an amide oxygen atom, generating [10 [Image: see text] ] chains in the crystal. [Image: see text] International Union of Crystallography 2022-02-25 /pmc/articles/PMC9462003/ /pubmed/36340874 http://dx.doi.org/10.1107/S2414314622002012 Text en © Hines III et al. 2022 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
Hines III, James E.
Deere, Curtistine J.
Fronczek, Frank R.
Uppu, Rao M.
N-(4-Hy­droxy-2-nitro­phen­yl)acetamide
title N-(4-Hy­droxy-2-nitro­phen­yl)acetamide
title_full N-(4-Hy­droxy-2-nitro­phen­yl)acetamide
title_fullStr N-(4-Hy­droxy-2-nitro­phen­yl)acetamide
title_full_unstemmed N-(4-Hy­droxy-2-nitro­phen­yl)acetamide
title_short N-(4-Hy­droxy-2-nitro­phen­yl)acetamide
title_sort n-(4-hy­droxy-2-nitro­phen­yl)acetamide
topic Data Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462003/
https://www.ncbi.nlm.nih.gov/pubmed/36340874
http://dx.doi.org/10.1107/S2414314622002012
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AT deerecurtistinej n4hydroxy2nitrophenylacetamide
AT fronczekfrankr n4hydroxy2nitrophenylacetamide
AT uppuraom n4hydroxy2nitrophenylacetamide

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