(E)-3-(2,6-Dichloro­benzyl­idene)indolin-2-one

There are two independent mol­ecules in the asymmetric unit of the title compound, C(15)H(9)Cl(2)NO. The dihedral angles between the oxindolyl and dichloro­phenyl rings are essentially identical for the two independent mol­ecules [63.4 (1) and 63.2 (1)°]. Dimers linked by amide–carbonyl N—H⋯O hydrog...

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Detalles Bibliográficos
Autores principales: Zhang, Hongming, Ankati, Haribabu, Biehl, Ed
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971081/
https://www.ncbi.nlm.nih.gov/pubmed/21578471
http://dx.doi.org/10.1107/S1600536809043487
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author Zhang, Hongming
Ankati, Haribabu
Biehl, Ed
author_facet Zhang, Hongming
Ankati, Haribabu
Biehl, Ed
author_sort Zhang, Hongming
collection PubMed
description There are two independent mol­ecules in the asymmetric unit of the title compound, C(15)H(9)Cl(2)NO. The dihedral angles between the oxindolyl and dichloro­phenyl rings are essentially identical for the two independent mol­ecules [63.4 (1) and 63.2 (1)°]. Dimers linked by amide–carbonyl N—H⋯O hydrogen bonds are formed from each symmetry-independent mol­ecule and the respective symmetry equivalent created by inversion.
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spelling pubmed-29710812010-12-30 (E)-3-(2,6-Dichloro­benzyl­idene)indolin-2-one Zhang, Hongming Ankati, Haribabu Biehl, Ed Acta Crystallogr Sect E Struct Rep Online Organic Papers There are two independent mol­ecules in the asymmetric unit of the title compound, C(15)H(9)Cl(2)NO. The dihedral angles between the oxindolyl and dichloro­phenyl rings are essentially identical for the two independent mol­ecules [63.4 (1) and 63.2 (1)°]. Dimers linked by amide–carbonyl N—H⋯O hydrogen bonds are formed from each symmetry-independent mol­ecule and the respective symmetry equivalent created by inversion. International Union of Crystallography 2009-10-28 /pmc/articles/PMC2971081/ /pubmed/21578471 http://dx.doi.org/10.1107/S1600536809043487 Text en © Zhang et al. 2009 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
Zhang, Hongming
Ankati, Haribabu
Biehl, Ed
(E)-3-(2,6-Dichloro­benzyl­idene)indolin-2-one
title (E)-3-(2,6-Dichloro­benzyl­idene)indolin-2-one
title_full (E)-3-(2,6-Dichloro­benzyl­idene)indolin-2-one
title_fullStr (E)-3-(2,6-Dichloro­benzyl­idene)indolin-2-one
title_full_unstemmed (E)-3-(2,6-Dichloro­benzyl­idene)indolin-2-one
title_short (E)-3-(2,6-Dichloro­benzyl­idene)indolin-2-one
title_sort (e)-3-(2,6-dichloro­benzyl­idene)indolin-2-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971081/
https://www.ncbi.nlm.nih.gov/pubmed/21578471
http://dx.doi.org/10.1107/S1600536809043487
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AT ankatiharibabu e326dichlorobenzylideneindolin2one
AT biehled e326dichlorobenzylideneindolin2one

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