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Methyl N′-[(E)-2-methoxybenzylidene]hydrazinecarboxylate
The title compound, C(10)H(12)N(2)O(3), crystallizes with two independent molecules in the asymmetric unit. The side chains in the two independent molecules have slightly different orientations, with the C=N—N—C torsion angle being 169.19 (14)° in one of the molecules and −179.86 (14)° in the oth...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977764/ https://www.ncbi.nlm.nih.gov/pubmed/21583900 http://dx.doi.org/10.1107/S1600536809014172 |
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author | Lv, Lu-Ping Yu, Wen-Bo Lu, Zhong-Hao Li, Wei-Wei Hu, Xian-Chao |
author_facet | Lv, Lu-Ping Yu, Wen-Bo Lu, Zhong-Hao Li, Wei-Wei Hu, Xian-Chao |
author_sort | Lv, Lu-Ping |
collection | PubMed |
description | The title compound, C(10)H(12)N(2)O(3), crystallizes with two independent molecules in the asymmetric unit. The side chains in the two independent molecules have slightly different orientations, with the C=N—N—C torsion angle being 169.19 (14)° in one of the molecules and −179.86 (14)° in the other. Each independent molecule adopts a trans configuration with respect to the C=N bond. In the crystal structure, molecules are linked into chains running along [001] by N—H⋯O, N—H⋯N and C—H⋯O hydrogen bonds. In addition, an intermolecular C—H⋯π interaction is observed. |
format | Text |
id | pubmed-2977764 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29777642010-12-30 Methyl N′-[(E)-2-methoxybenzylidene]hydrazinecarboxylate Lv, Lu-Ping Yu, Wen-Bo Lu, Zhong-Hao Li, Wei-Wei Hu, Xian-Chao Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(10)H(12)N(2)O(3), crystallizes with two independent molecules in the asymmetric unit. The side chains in the two independent molecules have slightly different orientations, with the C=N—N—C torsion angle being 169.19 (14)° in one of the molecules and −179.86 (14)° in the other. Each independent molecule adopts a trans configuration with respect to the C=N bond. In the crystal structure, molecules are linked into chains running along [001] by N—H⋯O, N—H⋯N and C—H⋯O hydrogen bonds. In addition, an intermolecular C—H⋯π interaction is observed. International Union of Crystallography 2009-04-22 /pmc/articles/PMC2977764/ /pubmed/21583900 http://dx.doi.org/10.1107/S1600536809014172 Text en © Lv 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 Lv, Lu-Ping Yu, Wen-Bo Lu, Zhong-Hao Li, Wei-Wei Hu, Xian-Chao Methyl N′-[(E)-2-methoxybenzylidene]hydrazinecarboxylate |
title | Methyl N′-[(E)-2-methoxybenzylidene]hydrazinecarboxylate |
title_full | Methyl N′-[(E)-2-methoxybenzylidene]hydrazinecarboxylate |
title_fullStr | Methyl N′-[(E)-2-methoxybenzylidene]hydrazinecarboxylate |
title_full_unstemmed | Methyl N′-[(E)-2-methoxybenzylidene]hydrazinecarboxylate |
title_short | Methyl N′-[(E)-2-methoxybenzylidene]hydrazinecarboxylate |
title_sort | methyl n′-[(e)-2-methoxybenzylidene]hydrazinecarboxylate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977764/ https://www.ncbi.nlm.nih.gov/pubmed/21583900 http://dx.doi.org/10.1107/S1600536809014172 |
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