2-Methyl­pyrazine 1,4-dioxide

The title compound, C(5)H(6)N(2)O(2), was prepared from 2-methyl­pyrazine, acetic acid and hydrogen peroxide. In the crystal, π–π stacking inter­actions between neighboring mol­ecules are observed, with a centroid–centroid distance of 3.7370 Å, an inter­planar distance of 3.167 Å, and a slippage of...

Descripción completa

Detalles Bibliográficos
Autores principales: Gratton, Jessica L., Knaust, Jacqueline M.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971871/
https://www.ncbi.nlm.nih.gov/pubmed/21578775
http://dx.doi.org/10.1107/S1600536809046534
_version_ 1782190689346387968
author Gratton, Jessica L.
Knaust, Jacqueline M.
author_facet Gratton, Jessica L.
Knaust, Jacqueline M.
author_sort Gratton, Jessica L.
collection PubMed
description The title compound, C(5)H(6)N(2)O(2), was prepared from 2-methyl­pyrazine, acetic acid and hydrogen peroxide. In the crystal, π–π stacking inter­actions between neighboring mol­ecules are observed, with a centroid–centroid distance of 3.7370 Å, an inter­planar distance of 3.167 Å, and a slippage of 1.984 Å. Each mol­ecule is linked to four neighbors through C—H⋯O hydrogen-bonding inter­actions, forming one-dimensional ribbons.
format Text
id pubmed-2971871
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29718712010-12-30 2-Methyl­pyrazine 1,4-dioxide Gratton, Jessica L. Knaust, Jacqueline M. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(5)H(6)N(2)O(2), was prepared from 2-methyl­pyrazine, acetic acid and hydrogen peroxide. In the crystal, π–π stacking inter­actions between neighboring mol­ecules are observed, with a centroid–centroid distance of 3.7370 Å, an inter­planar distance of 3.167 Å, and a slippage of 1.984 Å. Each mol­ecule is linked to four neighbors through C—H⋯O hydrogen-bonding inter­actions, forming one-dimensional ribbons. International Union of Crystallography 2009-11-07 /pmc/articles/PMC2971871/ /pubmed/21578775 http://dx.doi.org/10.1107/S1600536809046534 Text en © Gratton and Knaust 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
Gratton, Jessica L.
Knaust, Jacqueline M.
2-Methyl­pyrazine 1,4-dioxide
title 2-Methyl­pyrazine 1,4-dioxide
title_full 2-Methyl­pyrazine 1,4-dioxide
title_fullStr 2-Methyl­pyrazine 1,4-dioxide
title_full_unstemmed 2-Methyl­pyrazine 1,4-dioxide
title_short 2-Methyl­pyrazine 1,4-dioxide
title_sort 2-methyl­pyrazine 1,4-dioxide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971871/
https://www.ncbi.nlm.nih.gov/pubmed/21578775
http://dx.doi.org/10.1107/S1600536809046534
work_keys_str_mv AT grattonjessical 2methylpyrazine14dioxide
AT knaustjacquelinem 2methylpyrazine14dioxide

Ejemplares similares