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3-[2-(5-tert-Butyl-1,2-oxazol-3-yl)hydrazinylidene]chroman-2,4-dione
In the title compound, C(16)H(15)N(3)O(4), the dihedral angle between the chromane and isoxazole rings [r.m.s. deviations = 0.042 and 0.007 Å, respectively] is 20.33 (12)°. The molecular geometry is stabilized by an intramolecular N—H⋯O hydrogen bond. In the crystal, N—H⋯O hydrogen bonds generate...
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/PMC3569789/ https://www.ncbi.nlm.nih.gov/pubmed/23424535 http://dx.doi.org/10.1107/S1600536813000858 |
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author | Jashari, Ahmed Popovski, Emil Mikhova, Bozhana Nikolova, Rositsa P. Shivachev, Boris L. |
author_facet | Jashari, Ahmed Popovski, Emil Mikhova, Bozhana Nikolova, Rositsa P. Shivachev, Boris L. |
author_sort | Jashari, Ahmed |
collection | PubMed |
description | In the title compound, C(16)H(15)N(3)O(4), the dihedral angle between the chromane and isoxazole rings [r.m.s. deviations = 0.042 and 0.007 Å, respectively] is 20.33 (12)°. The molecular geometry is stabilized by an intramolecular N—H⋯O hydrogen bond. In the crystal, N—H⋯O hydrogen bonds generate chains along the c-axis direction. The crystal studied was a non-morohedral twin. |
format | Online Article Text |
id | pubmed-3569789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-35697892013-02-19 3-[2-(5-tert-Butyl-1,2-oxazol-3-yl)hydrazinylidene]chroman-2,4-dione Jashari, Ahmed Popovski, Emil Mikhova, Bozhana Nikolova, Rositsa P. Shivachev, Boris L. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(15)N(3)O(4), the dihedral angle between the chromane and isoxazole rings [r.m.s. deviations = 0.042 and 0.007 Å, respectively] is 20.33 (12)°. The molecular geometry is stabilized by an intramolecular N—H⋯O hydrogen bond. In the crystal, N—H⋯O hydrogen bonds generate chains along the c-axis direction. The crystal studied was a non-morohedral twin. International Union of Crystallography 2013-01-19 /pmc/articles/PMC3569789/ /pubmed/23424535 http://dx.doi.org/10.1107/S1600536813000858 Text en © Jashari 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 Jashari, Ahmed Popovski, Emil Mikhova, Bozhana Nikolova, Rositsa P. Shivachev, Boris L. 3-[2-(5-tert-Butyl-1,2-oxazol-3-yl)hydrazinylidene]chroman-2,4-dione |
title | 3-[2-(5-tert-Butyl-1,2-oxazol-3-yl)hydrazinylidene]chroman-2,4-dione |
title_full | 3-[2-(5-tert-Butyl-1,2-oxazol-3-yl)hydrazinylidene]chroman-2,4-dione |
title_fullStr | 3-[2-(5-tert-Butyl-1,2-oxazol-3-yl)hydrazinylidene]chroman-2,4-dione |
title_full_unstemmed | 3-[2-(5-tert-Butyl-1,2-oxazol-3-yl)hydrazinylidene]chroman-2,4-dione |
title_short | 3-[2-(5-tert-Butyl-1,2-oxazol-3-yl)hydrazinylidene]chroman-2,4-dione |
title_sort | 3-[2-(5-tert-butyl-1,2-oxazol-3-yl)hydrazinylidene]chroman-2,4-dione |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569789/ https://www.ncbi.nlm.nih.gov/pubmed/23424535 http://dx.doi.org/10.1107/S1600536813000858 |
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