2-Hydr­oxy-3,3-dimethyl-7-nitro-3,4-dihydro­isoquinolin-1(2H)-one

In the title compound, C(11)H(12)N(2)O(4), a new hydroxamic acid which belonging to the isoquinole family, the heterocyclic ring adopts a half-chair conformation. The nitro group is essentially coplanar with the aromatic ring. Inter­molecular O—H⋯O hydrogen bonds assemble the mol­ecules around inver...

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Detalles Bibliográficos
Autores principales: Ben Salah, Hassen, Kammoun, Majed, Hamdi, Besma, Bohé, Luis, Damak, Mohamed
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961355/
https://www.ncbi.nlm.nih.gov/pubmed/21202569
http://dx.doi.org/10.1107/S1600536808013457
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author Ben Salah, Hassen
Kammoun, Majed
Hamdi, Besma
Bohé, Luis
Damak, Mohamed
author_facet Ben Salah, Hassen
Kammoun, Majed
Hamdi, Besma
Bohé, Luis
Damak, Mohamed
author_sort Ben Salah, Hassen
collection PubMed
description In the title compound, C(11)H(12)N(2)O(4), a new hydroxamic acid which belonging to the isoquinole family, the heterocyclic ring adopts a half-chair conformation. The nitro group is essentially coplanar with the aromatic ring. Inter­molecular O—H⋯O hydrogen bonds assemble the mol­ecules around inversion centres to form pseudo-dimers.
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spelling pubmed-29613552010-12-30 2-Hydr­oxy-3,3-dimethyl-7-nitro-3,4-dihydro­isoquinolin-1(2H)-one Ben Salah, Hassen Kammoun, Majed Hamdi, Besma Bohé, Luis Damak, Mohamed Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(11)H(12)N(2)O(4), a new hydroxamic acid which belonging to the isoquinole family, the heterocyclic ring adopts a half-chair conformation. The nitro group is essentially coplanar with the aromatic ring. Inter­molecular O—H⋯O hydrogen bonds assemble the mol­ecules around inversion centres to form pseudo-dimers. International Union of Crystallography 2008-05-10 /pmc/articles/PMC2961355/ /pubmed/21202569 http://dx.doi.org/10.1107/S1600536808013457 Text en © Salah 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
Ben Salah, Hassen
Kammoun, Majed
Hamdi, Besma
Bohé, Luis
Damak, Mohamed
2-Hydr­oxy-3,3-dimethyl-7-nitro-3,4-dihydro­isoquinolin-1(2H)-one
title 2-Hydr­oxy-3,3-dimethyl-7-nitro-3,4-dihydro­isoquinolin-1(2H)-one
title_full 2-Hydr­oxy-3,3-dimethyl-7-nitro-3,4-dihydro­isoquinolin-1(2H)-one
title_fullStr 2-Hydr­oxy-3,3-dimethyl-7-nitro-3,4-dihydro­isoquinolin-1(2H)-one
title_full_unstemmed 2-Hydr­oxy-3,3-dimethyl-7-nitro-3,4-dihydro­isoquinolin-1(2H)-one
title_short 2-Hydr­oxy-3,3-dimethyl-7-nitro-3,4-dihydro­isoquinolin-1(2H)-one
title_sort 2-hydr­oxy-3,3-dimethyl-7-nitro-3,4-dihydro­isoquinolin-1(2h)-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961355/
https://www.ncbi.nlm.nih.gov/pubmed/21202569
http://dx.doi.org/10.1107/S1600536808013457
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AT damakmohamed 2hydroxy33dimethyl7nitro34dihydroisoquinolin12hone

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