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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...

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Detalles Bibliográficos
Autores principales: Kafka, Stanislav, Pevec, Andrej, Proisl, Karel, Kimmel, Roman, Košmrlj, Janez
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
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.
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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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