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N′-Hydroxypyridine-2-carboximidamide
The title molecule, C(6)H(7)N(3)O, is almost planar (r.m.s. deviation = 0.0068 Å) and adopts an E conformation about the C=N double bond. In the crystal, molecules are linked by pairs of strong N—H⋯N hydrogen bonds, forming inversion dimers with R (2) (2)(10) motifs. The dimers are further linked...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770436/ https://www.ncbi.nlm.nih.gov/pubmed/24046721 http://dx.doi.org/10.1107/S1600536813017418 |
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author | Suchetan, P. A. Sreenivasa, S. Palakshamurthy, B. S. Madhu Chakrapani Rao, T. Vijithkumar, |
author_facet | Suchetan, P. A. Sreenivasa, S. Palakshamurthy, B. S. Madhu Chakrapani Rao, T. Vijithkumar, |
author_sort | Suchetan, P. A. |
collection | PubMed |
description | The title molecule, C(6)H(7)N(3)O, is almost planar (r.m.s. deviation = 0.0068 Å) and adopts an E conformation about the C=N double bond. In the crystal, molecules are linked by pairs of strong N—H⋯N hydrogen bonds, forming inversion dimers with R (2) (2)(10) motifs. The dimers are further linked into C(3) chains through O—H⋯N hydrogen bonds. |
format | Online Article Text |
id | pubmed-3770436 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-37704362013-09-17 N′-Hydroxypyridine-2-carboximidamide Suchetan, P. A. Sreenivasa, S. Palakshamurthy, B. S. Madhu Chakrapani Rao, T. Vijithkumar, Acta Crystallogr Sect E Struct Rep Online Organic Papers The title molecule, C(6)H(7)N(3)O, is almost planar (r.m.s. deviation = 0.0068 Å) and adopts an E conformation about the C=N double bond. In the crystal, molecules are linked by pairs of strong N—H⋯N hydrogen bonds, forming inversion dimers with R (2) (2)(10) motifs. The dimers are further linked into C(3) chains through O—H⋯N hydrogen bonds. International Union of Crystallography 2013-06-29 /pmc/articles/PMC3770436/ /pubmed/24046721 http://dx.doi.org/10.1107/S1600536813017418 Text en © Suchetan et al. 2013 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 Suchetan, P. A. Sreenivasa, S. Palakshamurthy, B. S. Madhu Chakrapani Rao, T. Vijithkumar, N′-Hydroxypyridine-2-carboximidamide |
title |
N′-Hydroxypyridine-2-carboximidamide |
title_full |
N′-Hydroxypyridine-2-carboximidamide |
title_fullStr |
N′-Hydroxypyridine-2-carboximidamide |
title_full_unstemmed |
N′-Hydroxypyridine-2-carboximidamide |
title_short |
N′-Hydroxypyridine-2-carboximidamide |
title_sort | n′-hydroxypyridine-2-carboximidamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770436/ https://www.ncbi.nlm.nih.gov/pubmed/24046721 http://dx.doi.org/10.1107/S1600536813017418 |
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