4-Formyl-3-p-tolyl­sydnone

In the title compound, C(10)H(8)N(2)O(3), the oxadiazole ring is essentially planar, with a maximum deviation of 0.006 (1) Å for the two-connected N atom. The mean planes through the aldehyde unit and the methyl-substituted phenyl ring make inter­planar angles of 13.60 (9) and 59.69 (4)°, respective...

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Detalles Bibliográficos
Autores principales: Goh, Jia Hao, Fun, Hoong-Kun, Nithinchandra, Kalluraya, B.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979510/
https://www.ncbi.nlm.nih.gov/pubmed/21579399
http://dx.doi.org/10.1107/S1600536810016417
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author Goh, Jia Hao
Fun, Hoong-Kun
Nithinchandra,
Kalluraya, B.
author_facet Goh, Jia Hao
Fun, Hoong-Kun
Nithinchandra,
Kalluraya, B.
author_sort Goh, Jia Hao
collection PubMed
description In the title compound, C(10)H(8)N(2)O(3), the oxadiazole ring is essentially planar, with a maximum deviation of 0.006 (1) Å for the two-connected N atom. The mean planes through the aldehyde unit and the methyl-substituted phenyl ring make inter­planar angles of 13.60 (9) and 59.69 (4)°, respectively, with the oxadiazole ring. In the crystal structure, adjacent mol­ecules are inter­connected into a two-dimensional array parallel to (100) by inter­molecular C—H⋯O hydrogen bonds.
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spelling pubmed-29795102010-12-30 4-Formyl-3-p-tolyl­sydnone Goh, Jia Hao Fun, Hoong-Kun Nithinchandra, Kalluraya, B. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(10)H(8)N(2)O(3), the oxadiazole ring is essentially planar, with a maximum deviation of 0.006 (1) Å for the two-connected N atom. The mean planes through the aldehyde unit and the methyl-substituted phenyl ring make inter­planar angles of 13.60 (9) and 59.69 (4)°, respectively, with the oxadiazole ring. In the crystal structure, adjacent mol­ecules are inter­connected into a two-dimensional array parallel to (100) by inter­molecular C—H⋯O hydrogen bonds. International Union of Crystallography 2010-05-08 /pmc/articles/PMC2979510/ /pubmed/21579399 http://dx.doi.org/10.1107/S1600536810016417 Text en © Goh 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
Goh, Jia Hao
Fun, Hoong-Kun
Nithinchandra,
Kalluraya, B.
4-Formyl-3-p-tolyl­sydnone
title 4-Formyl-3-p-tolyl­sydnone
title_full 4-Formyl-3-p-tolyl­sydnone
title_fullStr 4-Formyl-3-p-tolyl­sydnone
title_full_unstemmed 4-Formyl-3-p-tolyl­sydnone
title_short 4-Formyl-3-p-tolyl­sydnone
title_sort 4-formyl-3-p-tolyl­sydnone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979510/
https://www.ncbi.nlm.nih.gov/pubmed/21579399
http://dx.doi.org/10.1107/S1600536810016417
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AT funhoongkun 4formyl3ptolylsydnone
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AT kallurayab 4formyl3ptolylsydnone

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