4-Meth­oxy­benzamidinium acetate

The title compound, C(8)H(11)N(2)O(+)·CH(3)CO(2) (−), was synthesized by a reaction between 4-meth­oxy­benzamidine (4-amidino­anisole) and acetic acid. In the cation, the amidinium group forms a dihedral angle of 11.65 (17)° with the mean plane of the benzene ring. The ionic components are associate...

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Detalles Bibliográficos
Autores principales: Irrera, Simona, Portalone, Gustavo
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/PMC3588825/
https://www.ncbi.nlm.nih.gov/pubmed/23468790
http://dx.doi.org/10.1107/S1600536812044911
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author Irrera, Simona
Portalone, Gustavo
author_facet Irrera, Simona
Portalone, Gustavo
author_sort Irrera, Simona
collection PubMed
description The title compound, C(8)H(11)N(2)O(+)·CH(3)CO(2) (−), was synthesized by a reaction between 4-meth­oxy­benzamidine (4-amidino­anisole) and acetic acid. In the cation, the amidinium group forms a dihedral angle of 11.65 (17)° with the mean plane of the benzene ring. The ionic components are associated in the crystal via N—H(+)⋯O(−) hydrogen bonds, resulting in a one-dimensional structure consisting of dimers and catemers and orientated approximately along the c axis.
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spelling pubmed-35888252013-03-06 4-Meth­oxy­benzamidinium acetate Irrera, Simona Portalone, Gustavo Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(8)H(11)N(2)O(+)·CH(3)CO(2) (−), was synthesized by a reaction between 4-meth­oxy­benzamidine (4-amidino­anisole) and acetic acid. In the cation, the amidinium group forms a dihedral angle of 11.65 (17)° with the mean plane of the benzene ring. The ionic components are associated in the crystal via N—H(+)⋯O(−) hydrogen bonds, resulting in a one-dimensional structure consisting of dimers and catemers and orientated approximately along the c axis. International Union of Crystallography 2012-11-03 /pmc/articles/PMC3588825/ /pubmed/23468790 http://dx.doi.org/10.1107/S1600536812044911 Text en © Irrera and Portalone 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
Irrera, Simona
Portalone, Gustavo
4-Meth­oxy­benzamidinium acetate
title 4-Meth­oxy­benzamidinium acetate
title_full 4-Meth­oxy­benzamidinium acetate
title_fullStr 4-Meth­oxy­benzamidinium acetate
title_full_unstemmed 4-Meth­oxy­benzamidinium acetate
title_short 4-Meth­oxy­benzamidinium acetate
title_sort 4-meth­oxy­benzamidinium acetate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588825/
https://www.ncbi.nlm.nih.gov/pubmed/23468790
http://dx.doi.org/10.1107/S1600536812044911
work_keys_str_mv AT irrerasimona 4methoxybenzamidiniumacetate
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