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Glycine methyl ester hydro­chloride

The title compound [systematic name: (methoxy­carbonyl­meth­yl)ammonium chloride], crystallizes as a salt, C(3)H(8)NO(2) (+)·Cl(−), with the charged species inter­acting mutually via strong and highly directional N(+)—H⋯Cl(−) hydrogen bonds which lead to the formation of a supra­molecular tape runni...

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Autores principales: Vilela, Sérgio M. F., Almeida Paz, Filipe A., Tomé, João P. C., de Zea Bermudez, Verónica, Cavaleiro, José A. S., Rocha, João
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977392/
https://www.ncbi.nlm.nih.gov/pubmed/21583646
http://dx.doi.org/10.1107/S1600536809028414
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author Vilela, Sérgio M. F.
Almeida Paz, Filipe A.
Tomé, João P. C.
de Zea Bermudez, Verónica
Cavaleiro, José A. S.
Rocha, João
author_facet Vilela, Sérgio M. F.
Almeida Paz, Filipe A.
Tomé, João P. C.
de Zea Bermudez, Verónica
Cavaleiro, José A. S.
Rocha, João
author_sort Vilela, Sérgio M. F.
collection PubMed
description The title compound [systematic name: (methoxy­carbonyl­meth­yl)ammonium chloride], crystallizes as a salt, C(3)H(8)NO(2) (+)·Cl(−), with the charged species inter­acting mutually via strong and highly directional N(+)—H⋯Cl(−) hydrogen bonds which lead to the formation of a supra­molecular tape running parallel to the c axis. Tapes close pack in the solid state mediated by multipoint recognition synthons based on weak C—H⋯O inter­actions and van der Waals contacts between adjacent methyl groups.
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spelling pubmed-29773922010-12-30 Glycine methyl ester hydro­chloride Vilela, Sérgio M. F. Almeida Paz, Filipe A. Tomé, João P. C. de Zea Bermudez, Verónica Cavaleiro, José A. S. Rocha, João Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound [systematic name: (methoxy­carbonyl­meth­yl)ammonium chloride], crystallizes as a salt, C(3)H(8)NO(2) (+)·Cl(−), with the charged species inter­acting mutually via strong and highly directional N(+)—H⋯Cl(−) hydrogen bonds which lead to the formation of a supra­molecular tape running parallel to the c axis. Tapes close pack in the solid state mediated by multipoint recognition synthons based on weak C—H⋯O inter­actions and van der Waals contacts between adjacent methyl groups. International Union of Crystallography 2009-07-25 /pmc/articles/PMC2977392/ /pubmed/21583646 http://dx.doi.org/10.1107/S1600536809028414 Text en © Vilela et al. 2009 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
Vilela, Sérgio M. F.
Almeida Paz, Filipe A.
Tomé, João P. C.
de Zea Bermudez, Verónica
Cavaleiro, José A. S.
Rocha, João
Glycine methyl ester hydro­chloride
title Glycine methyl ester hydro­chloride
title_full Glycine methyl ester hydro­chloride
title_fullStr Glycine methyl ester hydro­chloride
title_full_unstemmed Glycine methyl ester hydro­chloride
title_short Glycine methyl ester hydro­chloride
title_sort glycine methyl ester hydro­chloride
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977392/
https://www.ncbi.nlm.nih.gov/pubmed/21583646
http://dx.doi.org/10.1107/S1600536809028414
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