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2-Amino-3-[(E)-(2-hydroxy-3-methylbenzylidene)amino]but-2-enedinitrile
The title compound, C(12)H(10)N(4)O, is a Schiff base obtained from the condensation of diaminomaleonitrile and 2-hydroxy-3-methylbenzaldehyde. The molecule is roughly planar, with an r.m.s. deviation of 0.0354 Å, and adopts the phenol–imine tautomeric form. An intramolecular O—H⋯N hydrogen bon...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344532/ https://www.ncbi.nlm.nih.gov/pubmed/22590294 http://dx.doi.org/10.1107/S1600536812015243 |
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author | Aazam, Elham S. Büyükgüngör, Orhan |
author_facet | Aazam, Elham S. Büyükgüngör, Orhan |
author_sort | Aazam, Elham S. |
collection | PubMed |
description | The title compound, C(12)H(10)N(4)O, is a Schiff base obtained from the condensation of diaminomaleonitrile and 2-hydroxy-3-methylbenzaldehyde. The molecule is roughly planar, with an r.m.s. deviation of 0.0354 Å, and adopts the phenol–imine tautomeric form. An intramolecular O—H⋯N hydrogen bond involving the O—H group and the azomethine N atom generates an S(6) ring. In the crystal, there are two N—H⋯N hydrogen bonds. |
format | Online Article Text |
id | pubmed-3344532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-33445322012-05-15 2-Amino-3-[(E)-(2-hydroxy-3-methylbenzylidene)amino]but-2-enedinitrile Aazam, Elham S. Büyükgüngör, Orhan Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(12)H(10)N(4)O, is a Schiff base obtained from the condensation of diaminomaleonitrile and 2-hydroxy-3-methylbenzaldehyde. The molecule is roughly planar, with an r.m.s. deviation of 0.0354 Å, and adopts the phenol–imine tautomeric form. An intramolecular O—H⋯N hydrogen bond involving the O—H group and the azomethine N atom generates an S(6) ring. In the crystal, there are two N—H⋯N hydrogen bonds. International Union of Crystallography 2012-04-18 /pmc/articles/PMC3344532/ /pubmed/22590294 http://dx.doi.org/10.1107/S1600536812015243 Text en © Aazam and Büyükgüngör 2012 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 Aazam, Elham S. Büyükgüngör, Orhan 2-Amino-3-[(E)-(2-hydroxy-3-methylbenzylidene)amino]but-2-enedinitrile |
title | 2-Amino-3-[(E)-(2-hydroxy-3-methylbenzylidene)amino]but-2-enedinitrile |
title_full | 2-Amino-3-[(E)-(2-hydroxy-3-methylbenzylidene)amino]but-2-enedinitrile |
title_fullStr | 2-Amino-3-[(E)-(2-hydroxy-3-methylbenzylidene)amino]but-2-enedinitrile |
title_full_unstemmed | 2-Amino-3-[(E)-(2-hydroxy-3-methylbenzylidene)amino]but-2-enedinitrile |
title_short | 2-Amino-3-[(E)-(2-hydroxy-3-methylbenzylidene)amino]but-2-enedinitrile |
title_sort | 2-amino-3-[(e)-(2-hydroxy-3-methylbenzylidene)amino]but-2-enedinitrile |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344532/ https://www.ncbi.nlm.nih.gov/pubmed/22590294 http://dx.doi.org/10.1107/S1600536812015243 |
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