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N-(4-Chloro-3-methyl­phen­yl)succinamic acid

The title compound, C(11)H(12)ClNO(3), crystallizes with two independent mol­ecules in the asymmetric unit in which the dihedral angles between the benzene ring and the amide group are 55.0 (2) and 28.2 (3)°. The two independent mol­ecules are linked by an N—H⋯O hydrogen bond. In the crystal, mol­ec...

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Detalles Bibliográficos
Autores principales: Chaithanya, U., Foro, Sabine, Gowda, B. Thimme
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393275/
https://www.ncbi.nlm.nih.gov/pubmed/22807832
http://dx.doi.org/10.1107/S1600536812024567
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author Chaithanya, U.
Foro, Sabine
Gowda, B. Thimme
author_facet Chaithanya, U.
Foro, Sabine
Gowda, B. Thimme
author_sort Chaithanya, U.
collection PubMed
description The title compound, C(11)H(12)ClNO(3), crystallizes with two independent mol­ecules in the asymmetric unit in which the dihedral angles between the benzene ring and the amide group are 55.0 (2) and 28.2 (3)°. The two independent mol­ecules are linked by an N—H⋯O hydrogen bond. In the crystal, mol­ecules form inversion dimers via pairs of O—H⋯O hydrogen bonds. These dimers are linked into sheets parallel to (11-3) via N—H⋯O hydrogen bonds.
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spelling pubmed-33932752012-07-17 N-(4-Chloro-3-methyl­phen­yl)succinamic acid Chaithanya, U. Foro, Sabine Gowda, B. Thimme Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(11)H(12)ClNO(3), crystallizes with two independent mol­ecules in the asymmetric unit in which the dihedral angles between the benzene ring and the amide group are 55.0 (2) and 28.2 (3)°. The two independent mol­ecules are linked by an N—H⋯O hydrogen bond. In the crystal, mol­ecules form inversion dimers via pairs of O—H⋯O hydrogen bonds. These dimers are linked into sheets parallel to (11-3) via N—H⋯O hydrogen bonds. International Union of Crystallography 2012-06-13 /pmc/articles/PMC3393275/ /pubmed/22807832 http://dx.doi.org/10.1107/S1600536812024567 Text en © Chaithanya et al. 2012 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
Chaithanya, U.
Foro, Sabine
Gowda, B. Thimme
N-(4-Chloro-3-methyl­phen­yl)succinamic acid
title N-(4-Chloro-3-methyl­phen­yl)succinamic acid
title_full N-(4-Chloro-3-methyl­phen­yl)succinamic acid
title_fullStr N-(4-Chloro-3-methyl­phen­yl)succinamic acid
title_full_unstemmed N-(4-Chloro-3-methyl­phen­yl)succinamic acid
title_short N-(4-Chloro-3-methyl­phen­yl)succinamic acid
title_sort n-(4-chloro-3-methyl­phen­yl)succinamic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393275/
https://www.ncbi.nlm.nih.gov/pubmed/22807832
http://dx.doi.org/10.1107/S1600536812024567
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