5′,6-Dichloro-1′,3′,3′-trimethyl­spiro­[2H-1-benzopyran-2,2′-indoline]

In the crystal structure of the title compound, C(19)H(17)Cl(2)NO, the indoline and benzopyran ring systems are approximately perpendicular to each other. The indoline ring is in an envelope conformation with the spiro C atom as the flap. The N atom of the indoline ring forms a pyramidal environment...

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Detalles Bibliográficos
Autores principales: Alhashimy, Nameer, Müller-Bunz, Helge, Schazmann, Benjamin, Diamond, Dermot
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962063/
https://www.ncbi.nlm.nih.gov/pubmed/21203147
http://dx.doi.org/10.1107/S1600536808018722
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author Alhashimy, Nameer
Müller-Bunz, Helge
Schazmann, Benjamin
Diamond, Dermot
author_facet Alhashimy, Nameer
Müller-Bunz, Helge
Schazmann, Benjamin
Diamond, Dermot
author_sort Alhashimy, Nameer
collection PubMed
description In the crystal structure of the title compound, C(19)H(17)Cl(2)NO, the indoline and benzopyran ring systems are approximately perpendicular to each other. The indoline ring is in an envelope conformation with the spiro C atom as the flap. The N atom of the indoline ring forms a pyramidal environment, the sum of the angles at this atom being 352.46°.
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spelling pubmed-29620632010-12-30 5′,6-Dichloro-1′,3′,3′-trimethyl­spiro­[2H-1-benzopyran-2,2′-indoline] Alhashimy, Nameer Müller-Bunz, Helge Schazmann, Benjamin Diamond, Dermot Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(19)H(17)Cl(2)NO, the indoline and benzopyran ring systems are approximately perpendicular to each other. The indoline ring is in an envelope conformation with the spiro C atom as the flap. The N atom of the indoline ring forms a pyramidal environment, the sum of the angles at this atom being 352.46°. International Union of Crystallography 2008-07-09 /pmc/articles/PMC2962063/ /pubmed/21203147 http://dx.doi.org/10.1107/S1600536808018722 Text en © Alhashimy et al. 2008 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
Alhashimy, Nameer
Müller-Bunz, Helge
Schazmann, Benjamin
Diamond, Dermot
5′,6-Dichloro-1′,3′,3′-trimethyl­spiro­[2H-1-benzopyran-2,2′-indoline]
title 5′,6-Dichloro-1′,3′,3′-trimethyl­spiro­[2H-1-benzopyran-2,2′-indoline]
title_full 5′,6-Dichloro-1′,3′,3′-trimethyl­spiro­[2H-1-benzopyran-2,2′-indoline]
title_fullStr 5′,6-Dichloro-1′,3′,3′-trimethyl­spiro­[2H-1-benzopyran-2,2′-indoline]
title_full_unstemmed 5′,6-Dichloro-1′,3′,3′-trimethyl­spiro­[2H-1-benzopyran-2,2′-indoline]
title_short 5′,6-Dichloro-1′,3′,3′-trimethyl­spiro­[2H-1-benzopyran-2,2′-indoline]
title_sort 5′,6-dichloro-1′,3′,3′-trimethyl­spiro­[2h-1-benzopyran-2,2′-indoline]
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962063/
https://www.ncbi.nlm.nih.gov/pubmed/21203147
http://dx.doi.org/10.1107/S1600536808018722
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AT diamonddermot 56dichloro133trimethylspiro2h1benzopyran22indoline

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