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3-Acetyl-6-chloro-4-phenyl­quinolin-2(1H)-one

The title compound, C(17)H(12)ClNO(2), crystallizes with two mol­ecules in the asymmetric unit. The main conformational difference between these two mol­ecules is the dihedral angle between the phenyl ring and the quinoline ring system [70.5 (1)° and 65.5 (1) Å]. The crystal packing is stabilized by...

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Detalles Bibliográficos
Autores principales: Sundar, J. Kalyana, Natarajan, S., Sarveswari, S., Vijayakumar, V., Lakshman, P. L. Nilantha
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980191/
https://www.ncbi.nlm.nih.gov/pubmed/21580109
http://dx.doi.org/10.1107/S1600536809054087
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author Sundar, J. Kalyana
Natarajan, S.
Sarveswari, S.
Vijayakumar, V.
Lakshman, P. L. Nilantha
author_facet Sundar, J. Kalyana
Natarajan, S.
Sarveswari, S.
Vijayakumar, V.
Lakshman, P. L. Nilantha
author_sort Sundar, J. Kalyana
collection PubMed
description The title compound, C(17)H(12)ClNO(2), crystallizes with two mol­ecules in the asymmetric unit. The main conformational difference between these two mol­ecules is the dihedral angle between the phenyl ring and the quinoline ring system [70.5 (1)° and 65.5 (1) Å]. The crystal packing is stabilized by N—H⋯O hydrogen bonds.
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spelling pubmed-29801912010-12-30 3-Acetyl-6-chloro-4-phenyl­quinolin-2(1H)-one Sundar, J. Kalyana Natarajan, S. Sarveswari, S. Vijayakumar, V. Lakshman, P. L. Nilantha Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(17)H(12)ClNO(2), crystallizes with two mol­ecules in the asymmetric unit. The main conformational difference between these two mol­ecules is the dihedral angle between the phenyl ring and the quinoline ring system [70.5 (1)° and 65.5 (1) Å]. The crystal packing is stabilized by N—H⋯O hydrogen bonds. International Union of Crystallography 2009-12-24 /pmc/articles/PMC2980191/ /pubmed/21580109 http://dx.doi.org/10.1107/S1600536809054087 Text en © Sundar et al. 2010 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
Sundar, J. Kalyana
Natarajan, S.
Sarveswari, S.
Vijayakumar, V.
Lakshman, P. L. Nilantha
3-Acetyl-6-chloro-4-phenyl­quinolin-2(1H)-one
title 3-Acetyl-6-chloro-4-phenyl­quinolin-2(1H)-one
title_full 3-Acetyl-6-chloro-4-phenyl­quinolin-2(1H)-one
title_fullStr 3-Acetyl-6-chloro-4-phenyl­quinolin-2(1H)-one
title_full_unstemmed 3-Acetyl-6-chloro-4-phenyl­quinolin-2(1H)-one
title_short 3-Acetyl-6-chloro-4-phenyl­quinolin-2(1H)-one
title_sort 3-acetyl-6-chloro-4-phenyl­quinolin-2(1h)-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980191/
https://www.ncbi.nlm.nih.gov/pubmed/21580109
http://dx.doi.org/10.1107/S1600536809054087
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