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(RS)-1-[5-(2-Chloro­prop­yl)indolin-1-yl]ethanone

In the title compound, C(13)H(16)ClNO, the acetyl­indoline moiety is roughly planar (r.m.s. deviation = 0.0048 Å). The chloro­propyl group is out of the plane and is statistically disordered over two positions. Indeed, the Cl and CH(3) groups located on the stereogenic carbon exchange with each othe...

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Autor principal: Yang, Xue-Mei
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050396/
https://www.ncbi.nlm.nih.gov/pubmed/21522761
http://dx.doi.org/10.1107/S1600536810050476
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author Yang, Xue-Mei
author_facet Yang, Xue-Mei
author_sort Yang, Xue-Mei
collection PubMed
description In the title compound, C(13)H(16)ClNO, the acetyl­indoline moiety is roughly planar (r.m.s. deviation = 0.0048 Å). The chloro­propyl group is out of the plane and is statistically disordered over two positions. Indeed, the Cl and CH(3) groups located on the stereogenic carbon exchange with each other. The whole crystal is a racemate. Non-classical C—H⋯O hydrogen bonds between symmetry-related benzene rings stabilize the crystal structure.
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spelling pubmed-30503962011-04-26 (RS)-1-[5-(2-Chloro­prop­yl)indolin-1-yl]ethanone Yang, Xue-Mei Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(16)ClNO, the acetyl­indoline moiety is roughly planar (r.m.s. deviation = 0.0048 Å). The chloro­propyl group is out of the plane and is statistically disordered over two positions. Indeed, the Cl and CH(3) groups located on the stereogenic carbon exchange with each other. The whole crystal is a racemate. Non-classical C—H⋯O hydrogen bonds between symmetry-related benzene rings stabilize the crystal structure. International Union of Crystallography 2010-12-08 /pmc/articles/PMC3050396/ /pubmed/21522761 http://dx.doi.org/10.1107/S1600536810050476 Text en © Xue-Mei Yang 2011 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
Yang, Xue-Mei
(RS)-1-[5-(2-Chloro­prop­yl)indolin-1-yl]ethanone
title (RS)-1-[5-(2-Chloro­prop­yl)indolin-1-yl]ethanone
title_full (RS)-1-[5-(2-Chloro­prop­yl)indolin-1-yl]ethanone
title_fullStr (RS)-1-[5-(2-Chloro­prop­yl)indolin-1-yl]ethanone
title_full_unstemmed (RS)-1-[5-(2-Chloro­prop­yl)indolin-1-yl]ethanone
title_short (RS)-1-[5-(2-Chloro­prop­yl)indolin-1-yl]ethanone
title_sort (rs)-1-[5-(2-chloro­prop­yl)indolin-1-yl]ethanone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050396/
https://www.ncbi.nlm.nih.gov/pubmed/21522761
http://dx.doi.org/10.1107/S1600536810050476
work_keys_str_mv AT yangxuemei rs152chloropropylindolin1ylethanone