N-(2-Chloro-4-methyl­phen­yl)succinamic acid

In the title compound, C(11)H(12)ClNO(3), the N—C=O fragment is twisted from the plane of the attached benzene ring by 48.39 (12)°. The carb­oxy­lic acid group is involved in O—H⋯O hydrogen bonding, which links pairs of mol­ecules into centrosymmetric dimers. N—H⋯O hydrogen bonds link these dimers,...

Descripción completa

Detalles Bibliográficos
Autores principales: Chaithanya, U., Foro, Sabine, Gowda, B. Thimme
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297854/
https://www.ncbi.nlm.nih.gov/pubmed/22412657
http://dx.doi.org/10.1107/S1600536812005648
_version_ 1782225922519203840
author Chaithanya, U.
Foro, Sabine
Gowda, B. Thimme
author_facet Chaithanya, U.
Foro, Sabine
Gowda, B. Thimme
author_sort Chaithanya, U.
collection PubMed
description In the title compound, C(11)H(12)ClNO(3), the N—C=O fragment is twisted from the plane of the attached benzene ring by 48.39 (12)°. The carb­oxy­lic acid group is involved in O—H⋯O hydrogen bonding, which links pairs of mol­ecules into centrosymmetric dimers. N—H⋯O hydrogen bonds link these dimers, related by translation along the a axis, into ribbons.
format Online
Article
Text
id pubmed-3297854
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-32978542012-03-12 N-(2-Chloro-4-methyl­phen­yl)succinamic acid Chaithanya, U. Foro, Sabine Gowda, B. Thimme Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(11)H(12)ClNO(3), the N—C=O fragment is twisted from the plane of the attached benzene ring by 48.39 (12)°. The carb­oxy­lic acid group is involved in O—H⋯O hydrogen bonding, which links pairs of mol­ecules into centrosymmetric dimers. N—H⋯O hydrogen bonds link these dimers, related by translation along the a axis, into ribbons. International Union of Crystallography 2012-02-17 /pmc/articles/PMC3297854/ /pubmed/22412657 http://dx.doi.org/10.1107/S1600536812005648 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-(2-Chloro-4-methyl­phen­yl)succinamic acid
title N-(2-Chloro-4-methyl­phen­yl)succinamic acid
title_full N-(2-Chloro-4-methyl­phen­yl)succinamic acid
title_fullStr N-(2-Chloro-4-methyl­phen­yl)succinamic acid
title_full_unstemmed N-(2-Chloro-4-methyl­phen­yl)succinamic acid
title_short N-(2-Chloro-4-methyl­phen­yl)succinamic acid
title_sort n-(2-chloro-4-methyl­phen­yl)succinamic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297854/
https://www.ncbi.nlm.nih.gov/pubmed/22412657
http://dx.doi.org/10.1107/S1600536812005648
work_keys_str_mv AT chaithanyau n2chloro4methylphenylsuccinamicacid
AT forosabine n2chloro4methylphenylsuccinamicacid
AT gowdabthimme n2chloro4methylphenylsuccinamicacid

Ejemplares similares