1-Allyl-3-chloro-5-nitro-1H-indazole

In the title compound, C(10)H(8)ClN(3)O(2), the indazole ring system makes a dihedral angle of 7.9 (3)° with the plane through the nitro group. The allyl group is rotated out of the plane of the indazole ring system [N—N—C—C torsion angle = 104.28 (19)°]. In the crystal, mol­ecules are linked by C—H...

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Autores principales: Chicha, Hakima, Rakib, El Mostapha, Spinelli, Domenico, Saadi, Mohamed, El Ammari, Lahcen
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/PMC3884460/
https://www.ncbi.nlm.nih.gov/pubmed/24427047
http://dx.doi.org/10.1107/S1600536813021995
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author Chicha, Hakima
Rakib, El Mostapha
Spinelli, Domenico
Saadi, Mohamed
El Ammari, Lahcen
author_facet Chicha, Hakima
Rakib, El Mostapha
Spinelli, Domenico
Saadi, Mohamed
El Ammari, Lahcen
author_sort Chicha, Hakima
collection PubMed
description In the title compound, C(10)H(8)ClN(3)O(2), the indazole ring system makes a dihedral angle of 7.9 (3)° with the plane through the nitro group. The allyl group is rotated out of the plane of the indazole ring system [N—N—C—C torsion angle = 104.28 (19)°]. In the crystal, mol­ecules are linked by C—H⋯O hydrogen bonds, forming zigzag chains propagating along the b-axis direction.
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spelling pubmed-38844602014-01-14 1-Allyl-3-chloro-5-nitro-1H-indazole Chicha, Hakima Rakib, El Mostapha Spinelli, Domenico Saadi, Mohamed El Ammari, Lahcen Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(10)H(8)ClN(3)O(2), the indazole ring system makes a dihedral angle of 7.9 (3)° with the plane through the nitro group. The allyl group is rotated out of the plane of the indazole ring system [N—N—C—C torsion angle = 104.28 (19)°]. In the crystal, mol­ecules are linked by C—H⋯O hydrogen bonds, forming zigzag chains propagating along the b-axis direction. International Union of Crystallography 2013-08-10 /pmc/articles/PMC3884460/ /pubmed/24427047 http://dx.doi.org/10.1107/S1600536813021995 Text en © Chicha 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
Chicha, Hakima
Rakib, El Mostapha
Spinelli, Domenico
Saadi, Mohamed
El Ammari, Lahcen
1-Allyl-3-chloro-5-nitro-1H-indazole
title 1-Allyl-3-chloro-5-nitro-1H-indazole
title_full 1-Allyl-3-chloro-5-nitro-1H-indazole
title_fullStr 1-Allyl-3-chloro-5-nitro-1H-indazole
title_full_unstemmed 1-Allyl-3-chloro-5-nitro-1H-indazole
title_short 1-Allyl-3-chloro-5-nitro-1H-indazole
title_sort 1-allyl-3-chloro-5-nitro-1h-indazole
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884460/
https://www.ncbi.nlm.nih.gov/pubmed/24427047
http://dx.doi.org/10.1107/S1600536813021995
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AT spinellidomenico 1allyl3chloro5nitro1hindazole
AT saadimohamed 1allyl3chloro5nitro1hindazole
AT elammarilahcen 1allyl3chloro5nitro1hindazole

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