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4-Hydroxy-1-methyl-3-phenylquinolin-2(1H)-one
In the title compound, C(16)H(13)NO(2), the quinoline system is approximately planar with a maximum deviation from the least-squares plane of 0.059 (1) Å for the N atom. The phenyl ring is rotated by 62.16 (4)° with respect to the plane of the quinoline system. In the crystal, O—H⋯O hydrogen bonds l...
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/PMC3569765/ https://www.ncbi.nlm.nih.gov/pubmed/23424511 http://dx.doi.org/10.1107/S1600536813000226 |
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author | Kafka, Stanislav Pevec, Andrej Proisl, Karel Kimmel, Roman Košmrlj, Janez |
author_facet | Kafka, Stanislav Pevec, Andrej Proisl, Karel Kimmel, Roman Košmrlj, Janez |
author_sort | Kafka, Stanislav |
collection | PubMed |
description | In the title compound, C(16)H(13)NO(2), the quinoline system is approximately planar with a maximum deviation from the least-squares plane of 0.059 (1) Å for the N atom. The phenyl ring is rotated by 62.16 (4)° with respect to the plane of the quinoline system. In the crystal, O—H⋯O hydrogen bonds link molecules into infinite chains running along the b-axis direction. |
format | Online Article Text |
id | pubmed-3569765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-35697652013-02-19 4-Hydroxy-1-methyl-3-phenylquinolin-2(1H)-one Kafka, Stanislav Pevec, Andrej Proisl, Karel Kimmel, Roman Košmrlj, Janez Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(13)NO(2), the quinoline system is approximately planar with a maximum deviation from the least-squares plane of 0.059 (1) Å for the N atom. The phenyl ring is rotated by 62.16 (4)° with respect to the plane of the quinoline system. In the crystal, O—H⋯O hydrogen bonds link molecules into infinite chains running along the b-axis direction. International Union of Crystallography 2013-01-12 /pmc/articles/PMC3569765/ /pubmed/23424511 http://dx.doi.org/10.1107/S1600536813000226 Text en © Kafka 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 Kafka, Stanislav Pevec, Andrej Proisl, Karel Kimmel, Roman Košmrlj, Janez 4-Hydroxy-1-methyl-3-phenylquinolin-2(1H)-one |
title | 4-Hydroxy-1-methyl-3-phenylquinolin-2(1H)-one |
title_full | 4-Hydroxy-1-methyl-3-phenylquinolin-2(1H)-one |
title_fullStr | 4-Hydroxy-1-methyl-3-phenylquinolin-2(1H)-one |
title_full_unstemmed | 4-Hydroxy-1-methyl-3-phenylquinolin-2(1H)-one |
title_short | 4-Hydroxy-1-methyl-3-phenylquinolin-2(1H)-one |
title_sort | 4-hydroxy-1-methyl-3-phenylquinolin-2(1h)-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569765/ https://www.ncbi.nlm.nih.gov/pubmed/23424511 http://dx.doi.org/10.1107/S1600536813000226 |
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