N-(2,4,6-Trichloro­phen­yl)maleamic acid

In the crystal structure of the title compound, C(10)H(6)Cl(3)NO(3), the conformation of the amide bond is trans. The C=O and O—H bonds of the acid group are in the relatively rare anti position to each other. This is a consequence of the intra­molecular O—H⋯O hydrogen bond donated to the amide carb...

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Detalles Bibliográficos
Autores principales: Shakuntala, K., Foro, Sabine, Gowda, B. Thimme
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/PMC3213587/
https://www.ncbi.nlm.nih.gov/pubmed/22091164
http://dx.doi.org/10.1107/S1600536811029436
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author Shakuntala, K.
Foro, Sabine
Gowda, B. Thimme
author_facet Shakuntala, K.
Foro, Sabine
Gowda, B. Thimme
author_sort Shakuntala, K.
collection PubMed
description In the crystal structure of the title compound, C(10)H(6)Cl(3)NO(3), the conformation of the amide bond is trans. The C=O and O—H bonds of the acid group are in the relatively rare anti position to each other. This is a consequence of the intra­molecular O—H⋯O hydrogen bond donated to the amide carbonyl group stabilizing the mol­ecular structure. In the crystal, inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into zigzag chains along the c axis.
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spelling pubmed-32135872011-11-16 N-(2,4,6-Trichloro­phen­yl)maleamic acid Shakuntala, K. Foro, Sabine Gowda, B. Thimme Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(10)H(6)Cl(3)NO(3), the conformation of the amide bond is trans. The C=O and O—H bonds of the acid group are in the relatively rare anti position to each other. This is a consequence of the intra­molecular O—H⋯O hydrogen bond donated to the amide carbonyl group stabilizing the mol­ecular structure. In the crystal, inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into zigzag chains along the c axis. International Union of Crystallography 2011-07-30 /pmc/articles/PMC3213587/ /pubmed/22091164 http://dx.doi.org/10.1107/S1600536811029436 Text en © Shakuntala 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
Shakuntala, K.
Foro, Sabine
Gowda, B. Thimme
N-(2,4,6-Trichloro­phen­yl)maleamic acid
title N-(2,4,6-Trichloro­phen­yl)maleamic acid
title_full N-(2,4,6-Trichloro­phen­yl)maleamic acid
title_fullStr N-(2,4,6-Trichloro­phen­yl)maleamic acid
title_full_unstemmed N-(2,4,6-Trichloro­phen­yl)maleamic acid
title_short N-(2,4,6-Trichloro­phen­yl)maleamic acid
title_sort n-(2,4,6-trichloro­phen­yl)maleamic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213587/
https://www.ncbi.nlm.nih.gov/pubmed/22091164
http://dx.doi.org/10.1107/S1600536811029436
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AT gowdabthimme n246trichlorophenylmaleamicacid

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