o-Benzoquinone dioxime

The title compound, C(6)H(6)N(2)O(2), was obtained as a product of an in vitro study of the metabolism of benzofuroxan. The molecule exhibits a amphi configuration of the oxime groups C=N—OH. One oxime group is involved in the formation of a strong intra­molecular O—H⋯N hydrogen bond, while another...

Descripción completa

Detalles Bibliográficos
Autores principales: Gervasio, Giuliana, Marabello, Domenica, Bertolotti, Federica
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009110/
https://www.ncbi.nlm.nih.gov/pubmed/21588966
http://dx.doi.org/10.1107/S1600536810039619
_version_ 1782194609132142592
author Gervasio, Giuliana
Marabello, Domenica
Bertolotti, Federica
author_facet Gervasio, Giuliana
Marabello, Domenica
Bertolotti, Federica
author_sort Gervasio, Giuliana
collection PubMed
description The title compound, C(6)H(6)N(2)O(2), was obtained as a product of an in vitro study of the metabolism of benzofuroxan. The molecule exhibits a amphi configuration of the oxime groups C=N—OH. One oxime group is involved in the formation of a strong intra­molecular O—H⋯N hydrogen bond, while another links mol­ecules into zigzag chains along the c axis via inter­molecular O—H⋯N hydrogen bonds.
format Text
id pubmed-3009110
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-30091102010-12-30 o-Benzoquinone dioxime Gervasio, Giuliana Marabello, Domenica Bertolotti, Federica Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(6)H(6)N(2)O(2), was obtained as a product of an in vitro study of the metabolism of benzofuroxan. The molecule exhibits a amphi configuration of the oxime groups C=N—OH. One oxime group is involved in the formation of a strong intra­molecular O—H⋯N hydrogen bond, while another links mol­ecules into zigzag chains along the c axis via inter­molecular O—H⋯N hydrogen bonds. International Union of Crystallography 2010-10-09 /pmc/articles/PMC3009110/ /pubmed/21588966 http://dx.doi.org/10.1107/S1600536810039619 Text en © Gervasio et al. 2010 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
Gervasio, Giuliana
Marabello, Domenica
Bertolotti, Federica
o-Benzoquinone dioxime
title o-Benzoquinone dioxime
title_full o-Benzoquinone dioxime
title_fullStr o-Benzoquinone dioxime
title_full_unstemmed o-Benzoquinone dioxime
title_short o-Benzoquinone dioxime
title_sort o-benzoquinone dioxime
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009110/
https://www.ncbi.nlm.nih.gov/pubmed/21588966
http://dx.doi.org/10.1107/S1600536810039619
work_keys_str_mv AT gervasiogiuliana obenzoquinonedioxime
AT marabellodomenica obenzoquinonedioxime
AT bertolottifederica obenzoquinonedioxime

Ejemplares similares