N-(4-Methyl­phen­yl)succinamic acid

In the title compound, C(11)H(13)NO(3), the conformations of the N—H and C=O bonds in the amide segment are anti to each other. Further, the conformations of the amide and carbonyl O atoms of the acid segment are also anti to the adjacent –CH(2) groups. The C=O and O—H bonds of the acid group are sy...

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Detalles Bibliográficos
Autores principales: Saraswathi, B. S., Foro, Sabine, Gowda, B. Thimme, Fuess, Hartmut
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050143/
https://www.ncbi.nlm.nih.gov/pubmed/21522726
http://dx.doi.org/10.1107/S1600536810053298
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author Saraswathi, B. S.
Foro, Sabine
Gowda, B. Thimme
Fuess, Hartmut
author_facet Saraswathi, B. S.
Foro, Sabine
Gowda, B. Thimme
Fuess, Hartmut
author_sort Saraswathi, B. S.
collection PubMed
description In the title compound, C(11)H(13)NO(3), the conformations of the N—H and C=O bonds in the amide segment are anti to each other. Further, the conformations of the amide and carbonyl O atoms of the acid segment are also anti to the adjacent –CH(2) groups. The C=O and O—H bonds of the acid group are syn to each other. In the crystal, mol­ecules are packed into infinite chains along the b axis through inter­molecular N—H⋯O and O—H⋯O hydrogen bonds.
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spelling pubmed-30501432011-04-26 N-(4-Methyl­phen­yl)succinamic acid Saraswathi, B. S. Foro, Sabine Gowda, B. Thimme Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(11)H(13)NO(3), the conformations of the N—H and C=O bonds in the amide segment are anti to each other. Further, the conformations of the amide and carbonyl O atoms of the acid segment are also anti to the adjacent –CH(2) groups. The C=O and O—H bonds of the acid group are syn to each other. In the crystal, mol­ecules are packed into infinite chains along the b axis through inter­molecular N—H⋯O and O—H⋯O hydrogen bonds. International Union of Crystallography 2010-12-24 /pmc/articles/PMC3050143/ /pubmed/21522726 http://dx.doi.org/10.1107/S1600536810053298 Text en © Saraswathi 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
Saraswathi, B. S.
Foro, Sabine
Gowda, B. Thimme
Fuess, Hartmut
N-(4-Methyl­phen­yl)succinamic acid
title N-(4-Methyl­phen­yl)succinamic acid
title_full N-(4-Methyl­phen­yl)succinamic acid
title_fullStr N-(4-Methyl­phen­yl)succinamic acid
title_full_unstemmed N-(4-Methyl­phen­yl)succinamic acid
title_short N-(4-Methyl­phen­yl)succinamic acid
title_sort n-(4-methyl­phen­yl)succinamic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050143/
https://www.ncbi.nlm.nih.gov/pubmed/21522726
http://dx.doi.org/10.1107/S1600536810053298
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