5-Chloro­quinolin-8-yl furan-2-carboxyl­ate

In the title compound, C(14)H(8)ClNO(3), the central ester CO(2) group is twisted away from the quinoline and furoyl rings by 57.46 (5) and 2.0 (1)°, respectively. In the crystal, mol­ecules are linked by weak C—H⋯O inter­actions, forming chains in [001].

Detalles Bibliográficos
Autores principales: Moreno-Fuquen, Rodolfo, Hernandez, Geraldine, Ellena, Javier, De Simone, Carlos A., Tenorio, Juan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3629531/
https://www.ncbi.nlm.nih.gov/pubmed/23634049
http://dx.doi.org/10.1107/S1600536813005667
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author Moreno-Fuquen, Rodolfo
Hernandez, Geraldine
Ellena, Javier
De Simone, Carlos A.
Tenorio, Juan C.
author_facet Moreno-Fuquen, Rodolfo
Hernandez, Geraldine
Ellena, Javier
De Simone, Carlos A.
Tenorio, Juan C.
author_sort Moreno-Fuquen, Rodolfo
collection PubMed
description In the title compound, C(14)H(8)ClNO(3), the central ester CO(2) group is twisted away from the quinoline and furoyl rings by 57.46 (5) and 2.0 (1)°, respectively. In the crystal, mol­ecules are linked by weak C—H⋯O inter­actions, forming chains in [001].
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spelling pubmed-36295312013-04-30 5-Chloro­quinolin-8-yl furan-2-carboxyl­ate Moreno-Fuquen, Rodolfo Hernandez, Geraldine Ellena, Javier De Simone, Carlos A. Tenorio, Juan C. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(14)H(8)ClNO(3), the central ester CO(2) group is twisted away from the quinoline and furoyl rings by 57.46 (5) and 2.0 (1)°, respectively. In the crystal, mol­ecules are linked by weak C—H⋯O inter­actions, forming chains in [001]. International Union of Crystallography 2013-03-06 /pmc/articles/PMC3629531/ /pubmed/23634049 http://dx.doi.org/10.1107/S1600536813005667 Text en © Moreno-Fuquen 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
Moreno-Fuquen, Rodolfo
Hernandez, Geraldine
Ellena, Javier
De Simone, Carlos A.
Tenorio, Juan C.
5-Chloro­quinolin-8-yl furan-2-carboxyl­ate
title 5-Chloro­quinolin-8-yl furan-2-carboxyl­ate
title_full 5-Chloro­quinolin-8-yl furan-2-carboxyl­ate
title_fullStr 5-Chloro­quinolin-8-yl furan-2-carboxyl­ate
title_full_unstemmed 5-Chloro­quinolin-8-yl furan-2-carboxyl­ate
title_short 5-Chloro­quinolin-8-yl furan-2-carboxyl­ate
title_sort 5-chloro­quinolin-8-yl furan-2-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3629531/
https://www.ncbi.nlm.nih.gov/pubmed/23634049
http://dx.doi.org/10.1107/S1600536813005667
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