N-Nitro-1H-pyrrole-2-carboxamide

In the title compound, C(5)H(5)N(3)O(3), the nitro group is twisted with respect to the amide group, with C—N—N—O torsion angles of 29.0 (2) and −153.66 (14)°. In the crystal, mol­ecules are linked through inter­molecular N—H⋯O and C—H⋯O hydrogen bonds, forming supra­molecular chains along the a axi...

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Autores principales: Liu, Long, He, Chunlin, Li, Zengxi, Li, Chunshan, Zhang, Xiangping, Zhang, Suojiang
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051632/
https://www.ncbi.nlm.nih.gov/pubmed/21523136
http://dx.doi.org/10.1107/S1600536811002455
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author Liu, Long
He, Chunlin
Li, Zengxi
Li, Chunshan
Zhang, Xiangping
Zhang, Suojiang
author_facet Liu, Long
He, Chunlin
Li, Zengxi
Li, Chunshan
Zhang, Xiangping
Zhang, Suojiang
author_sort Liu, Long
collection PubMed
description In the title compound, C(5)H(5)N(3)O(3), the nitro group is twisted with respect to the amide group, with C—N—N—O torsion angles of 29.0 (2) and −153.66 (14)°. In the crystal, mol­ecules are linked through inter­molecular N—H⋯O and C—H⋯O hydrogen bonds, forming supra­molecular chains along the a axis. These chains stack in parallel and form distinct layer motifs in the (001) plane.
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spelling pubmed-30516322011-04-26 N-Nitro-1H-pyrrole-2-carboxamide Liu, Long He, Chunlin Li, Zengxi Li, Chunshan Zhang, Xiangping Zhang, Suojiang Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(5)H(5)N(3)O(3), the nitro group is twisted with respect to the amide group, with C—N—N—O torsion angles of 29.0 (2) and −153.66 (14)°. In the crystal, mol­ecules are linked through inter­molecular N—H⋯O and C—H⋯O hydrogen bonds, forming supra­molecular chains along the a axis. These chains stack in parallel and form distinct layer motifs in the (001) plane. International Union of Crystallography 2011-01-22 /pmc/articles/PMC3051632/ /pubmed/21523136 http://dx.doi.org/10.1107/S1600536811002455 Text en © Liu et al. 2011 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
Liu, Long
He, Chunlin
Li, Zengxi
Li, Chunshan
Zhang, Xiangping
Zhang, Suojiang
N-Nitro-1H-pyrrole-2-carboxamide
title N-Nitro-1H-pyrrole-2-carboxamide
title_full N-Nitro-1H-pyrrole-2-carboxamide
title_fullStr N-Nitro-1H-pyrrole-2-carboxamide
title_full_unstemmed N-Nitro-1H-pyrrole-2-carboxamide
title_short N-Nitro-1H-pyrrole-2-carboxamide
title_sort n-nitro-1h-pyrrole-2-carboxamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051632/
https://www.ncbi.nlm.nih.gov/pubmed/21523136
http://dx.doi.org/10.1107/S1600536811002455
work_keys_str_mv AT liulong nnitro1hpyrrole2carboxamide
AT hechunlin nnitro1hpyrrole2carboxamide
AT lizengxi nnitro1hpyrrole2carboxamide
AT lichunshan nnitro1hpyrrole2carboxamide
AT zhangxiangping nnitro1hpyrrole2carboxamide
AT zhangsuojiang nnitro1hpyrrole2carboxamide

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