Methyl 1H-pyrrole-2-carboxyl­ate

The title compound, C(6)H(7)NO(2), is essentially planar with a dihedral angle of 3.6 (3)° between the pyrrole ring and the methoxy­carbonyl O/C/O/C plane. In the crystal structure, the N atom is a hydrogen-bond donor to the carboxylate C=O O atom of the neighboring mol­ecule. These inter­molecular...

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Detalles Bibliográficos
Autores principales: Kerscher, Tobias, Mayer, Peter, Klüfers, Peter
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970022/
https://www.ncbi.nlm.nih.gov/pubmed/21577598
http://dx.doi.org/10.1107/S1600536809030906
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author Kerscher, Tobias
Mayer, Peter
Klüfers, Peter
author_facet Kerscher, Tobias
Mayer, Peter
Klüfers, Peter
author_sort Kerscher, Tobias
collection PubMed
description The title compound, C(6)H(7)NO(2), is essentially planar with a dihedral angle of 3.6 (3)° between the pyrrole ring and the methoxy­carbonyl O/C/O/C plane. In the crystal structure, the N atom is a hydrogen-bond donor to the carboxylate C=O O atom of the neighboring mol­ecule. These inter­molecular hydrogen bonds lead to the formation of helical chains along the b axis.
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spelling pubmed-29700222010-12-30 Methyl 1H-pyrrole-2-carboxyl­ate Kerscher, Tobias Mayer, Peter Klüfers, Peter Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(6)H(7)NO(2), is essentially planar with a dihedral angle of 3.6 (3)° between the pyrrole ring and the methoxy­carbonyl O/C/O/C plane. In the crystal structure, the N atom is a hydrogen-bond donor to the carboxylate C=O O atom of the neighboring mol­ecule. These inter­molecular hydrogen bonds lead to the formation of helical chains along the b axis. International Union of Crystallography 2009-08-19 /pmc/articles/PMC2970022/ /pubmed/21577598 http://dx.doi.org/10.1107/S1600536809030906 Text en © Kerscher 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
Kerscher, Tobias
Mayer, Peter
Klüfers, Peter
Methyl 1H-pyrrole-2-carboxyl­ate
title Methyl 1H-pyrrole-2-carboxyl­ate
title_full Methyl 1H-pyrrole-2-carboxyl­ate
title_fullStr Methyl 1H-pyrrole-2-carboxyl­ate
title_full_unstemmed Methyl 1H-pyrrole-2-carboxyl­ate
title_short Methyl 1H-pyrrole-2-carboxyl­ate
title_sort methyl 1h-pyrrole-2-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970022/
https://www.ncbi.nlm.nih.gov/pubmed/21577598
http://dx.doi.org/10.1107/S1600536809030906
work_keys_str_mv AT kerschertobias methyl1hpyrrole2carboxylate
AT mayerpeter methyl1hpyrrole2carboxylate
AT kluferspeter methyl1hpyrrole2carboxylate

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