2-Amino-4-methyl­pyridinium 2-carb­oxy­benzoate

In the title mol­ecular salt, C(6)H(9)N(2) (+)·C(8)H(5)O(4) (−), the anion is stabilized by an intra­molecular O—H⋯O hydrogen bond, which generates an S(7) ring motif. In the crystal, the cations and anions are linked to form extended chains along [001] by O—H⋯O and N—H⋯O hydrogen bonds. Adjacent ch...

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Detalles Bibliográficos
Autores principales: Quah, Ching Kheng, Hemamalini, Madhukar, Fun, Hoong-Kun
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007269/
https://www.ncbi.nlm.nih.gov/pubmed/21588261
http://dx.doi.org/10.1107/S1600536810025900
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author Quah, Ching Kheng
Hemamalini, Madhukar
Fun, Hoong-Kun
author_facet Quah, Ching Kheng
Hemamalini, Madhukar
Fun, Hoong-Kun
author_sort Quah, Ching Kheng
collection PubMed
description In the title mol­ecular salt, C(6)H(9)N(2) (+)·C(8)H(5)O(4) (−), the anion is stabilized by an intra­molecular O—H⋯O hydrogen bond, which generates an S(7) ring motif. In the crystal, the cations and anions are linked to form extended chains along [001] by O—H⋯O and N—H⋯O hydrogen bonds. Adjacent chains are crosslinked via C—H⋯O inter­actions into sheets lying parallel to (100).
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spelling pubmed-30072692010-12-30 2-Amino-4-methyl­pyridinium 2-carb­oxy­benzoate Quah, Ching Kheng Hemamalini, Madhukar Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title mol­ecular salt, C(6)H(9)N(2) (+)·C(8)H(5)O(4) (−), the anion is stabilized by an intra­molecular O—H⋯O hydrogen bond, which generates an S(7) ring motif. In the crystal, the cations and anions are linked to form extended chains along [001] by O—H⋯O and N—H⋯O hydrogen bonds. Adjacent chains are crosslinked via C—H⋯O inter­actions into sheets lying parallel to (100). International Union of Crystallography 2010-07-07 /pmc/articles/PMC3007269/ /pubmed/21588261 http://dx.doi.org/10.1107/S1600536810025900 Text en © Quah et al. 2010 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
Quah, Ching Kheng
Hemamalini, Madhukar
Fun, Hoong-Kun
2-Amino-4-methyl­pyridinium 2-carb­oxy­benzoate
title 2-Amino-4-methyl­pyridinium 2-carb­oxy­benzoate
title_full 2-Amino-4-methyl­pyridinium 2-carb­oxy­benzoate
title_fullStr 2-Amino-4-methyl­pyridinium 2-carb­oxy­benzoate
title_full_unstemmed 2-Amino-4-methyl­pyridinium 2-carb­oxy­benzoate
title_short 2-Amino-4-methyl­pyridinium 2-carb­oxy­benzoate
title_sort 2-amino-4-methyl­pyridinium 2-carb­oxy­benzoate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007269/
https://www.ncbi.nlm.nih.gov/pubmed/21588261
http://dx.doi.org/10.1107/S1600536810025900
work_keys_str_mv AT quahchingkheng 2amino4methylpyridinium2carboxybenzoate
AT hemamalinimadhukar 2amino4methylpyridinium2carboxybenzoate
AT funhoongkun 2amino4methylpyridinium2carboxybenzoate

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