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1-[3-(4-Nitro­phen­yl)propano­yl]urea acetic acid monosolvate

The title compound, C(10)H(11)N(3)O(4)·C(2)H(4)O(2), was prepared by an electrochemical technique. In the crystal, acetic acid mol­ecules are involved in hydrogen bonding to two separate propano­ylurea mol­ecules, acting as a donor in an O—H⋯O inter­action and as an acceptor in two N—H⋯O inter­actio...

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Autores principales: Merzouki, Soraya, Mouats, Chabane, Bendeif, El-Eulmi, Pillet, Sebastien, Bouchouit, Karim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247309/
https://www.ncbi.nlm.nih.gov/pubmed/22219927
http://dx.doi.org/10.1107/S1600536811039729
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author Merzouki, Soraya
Mouats, Chabane
Bendeif, El-Eulmi
Pillet, Sebastien
Bouchouit, Karim
author_facet Merzouki, Soraya
Mouats, Chabane
Bendeif, El-Eulmi
Pillet, Sebastien
Bouchouit, Karim
author_sort Merzouki, Soraya
collection PubMed
description The title compound, C(10)H(11)N(3)O(4)·C(2)H(4)O(2), was prepared by an electrochemical technique. In the crystal, acetic acid mol­ecules are involved in hydrogen bonding to two separate propano­ylurea mol­ecules, acting as a donor in an O—H⋯O inter­action and as an acceptor in two N—H⋯O inter­actions. The propano­ylurea mol­ecules inter­act with each other via N—H⋯O hydrogen bonds. C—H⋯O inter­actions also stabilize the crystal structure.
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spelling pubmed-32473092012-01-04 1-[3-(4-Nitro­phen­yl)propano­yl]urea acetic acid monosolvate Merzouki, Soraya Mouats, Chabane Bendeif, El-Eulmi Pillet, Sebastien Bouchouit, Karim Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(10)H(11)N(3)O(4)·C(2)H(4)O(2), was prepared by an electrochemical technique. In the crystal, acetic acid mol­ecules are involved in hydrogen bonding to two separate propano­ylurea mol­ecules, acting as a donor in an O—H⋯O inter­action and as an acceptor in two N—H⋯O inter­actions. The propano­ylurea mol­ecules inter­act with each other via N—H⋯O hydrogen bonds. C—H⋯O inter­actions also stabilize the crystal structure. International Union of Crystallography 2011-10-08 /pmc/articles/PMC3247309/ /pubmed/22219927 http://dx.doi.org/10.1107/S1600536811039729 Text en © Merzouki 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
Merzouki, Soraya
Mouats, Chabane
Bendeif, El-Eulmi
Pillet, Sebastien
Bouchouit, Karim
1-[3-(4-Nitro­phen­yl)propano­yl]urea acetic acid monosolvate
title 1-[3-(4-Nitro­phen­yl)propano­yl]urea acetic acid monosolvate
title_full 1-[3-(4-Nitro­phen­yl)propano­yl]urea acetic acid monosolvate
title_fullStr 1-[3-(4-Nitro­phen­yl)propano­yl]urea acetic acid monosolvate
title_full_unstemmed 1-[3-(4-Nitro­phen­yl)propano­yl]urea acetic acid monosolvate
title_short 1-[3-(4-Nitro­phen­yl)propano­yl]urea acetic acid monosolvate
title_sort 1-[3-(4-nitro­phen­yl)propano­yl]urea acetic acid monosolvate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247309/
https://www.ncbi.nlm.nih.gov/pubmed/22219927
http://dx.doi.org/10.1107/S1600536811039729
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