2,3-Dibromo-3-(4-bromo­phen­yl)-1-[3-(4-meth­oxy­phen­yl)sydnon-4-yl]propan-1-one

In the title compound {systematic name: 4-[2,3-dibromo-3-(4-bromo­phen­yl)propano­yl]-3-(4-meth­oxy­phen­yl)-1,2,3-oxa­dia­zol-3-ylium-5-olate}, C(18)H(13)Br(3)N(2)O(4), the central oxadiazole ring, which is essentially planar with a maximum deviation of 0.016 (3) Å, makes dihedral angles of 29.98 (...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Hemamalini, Madhukar, Nithinchandra, Kalluraya, Balakrishna
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3099938/
https://www.ncbi.nlm.nih.gov/pubmed/21754217
http://dx.doi.org/10.1107/S1600536811010002
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author Fun, Hoong-Kun
Hemamalini, Madhukar
Nithinchandra,
Kalluraya, Balakrishna
author_facet Fun, Hoong-Kun
Hemamalini, Madhukar
Nithinchandra,
Kalluraya, Balakrishna
author_sort Fun, Hoong-Kun
collection PubMed
description In the title compound {systematic name: 4-[2,3-dibromo-3-(4-bromo­phen­yl)propano­yl]-3-(4-meth­oxy­phen­yl)-1,2,3-oxa­dia­zol-3-ylium-5-olate}, C(18)H(13)Br(3)N(2)O(4), the central oxadiazole ring, which is essentially planar with a maximum deviation of 0.016 (3) Å, makes dihedral angles of 29.98 (16) and 52.04 (16)°, respectively, with the terminal bromo-substituted and meth­oxy-substituted benzene rings. An intra­molecular C—H⋯O hydrogen bond generates an S(6) ring motif.
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spelling pubmed-30999382011-07-13 2,3-Dibromo-3-(4-bromo­phen­yl)-1-[3-(4-meth­oxy­phen­yl)sydnon-4-yl]propan-1-one Fun, Hoong-Kun Hemamalini, Madhukar Nithinchandra, Kalluraya, Balakrishna Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound {systematic name: 4-[2,3-dibromo-3-(4-bromo­phen­yl)propano­yl]-3-(4-meth­oxy­phen­yl)-1,2,3-oxa­dia­zol-3-ylium-5-olate}, C(18)H(13)Br(3)N(2)O(4), the central oxadiazole ring, which is essentially planar with a maximum deviation of 0.016 (3) Å, makes dihedral angles of 29.98 (16) and 52.04 (16)°, respectively, with the terminal bromo-substituted and meth­oxy-substituted benzene rings. An intra­molecular C—H⋯O hydrogen bond generates an S(6) ring motif. International Union of Crystallography 2011-03-23 /pmc/articles/PMC3099938/ /pubmed/21754217 http://dx.doi.org/10.1107/S1600536811010002 Text en © Fun et al. 2011 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
Fun, Hoong-Kun
Hemamalini, Madhukar
Nithinchandra,
Kalluraya, Balakrishna
2,3-Dibromo-3-(4-bromo­phen­yl)-1-[3-(4-meth­oxy­phen­yl)sydnon-4-yl]propan-1-one
title 2,3-Dibromo-3-(4-bromo­phen­yl)-1-[3-(4-meth­oxy­phen­yl)sydnon-4-yl]propan-1-one
title_full 2,3-Dibromo-3-(4-bromo­phen­yl)-1-[3-(4-meth­oxy­phen­yl)sydnon-4-yl]propan-1-one
title_fullStr 2,3-Dibromo-3-(4-bromo­phen­yl)-1-[3-(4-meth­oxy­phen­yl)sydnon-4-yl]propan-1-one
title_full_unstemmed 2,3-Dibromo-3-(4-bromo­phen­yl)-1-[3-(4-meth­oxy­phen­yl)sydnon-4-yl]propan-1-one
title_short 2,3-Dibromo-3-(4-bromo­phen­yl)-1-[3-(4-meth­oxy­phen­yl)sydnon-4-yl]propan-1-one
title_sort 2,3-dibromo-3-(4-bromo­phen­yl)-1-[3-(4-meth­oxy­phen­yl)sydnon-4-yl]propan-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3099938/
https://www.ncbi.nlm.nih.gov/pubmed/21754217
http://dx.doi.org/10.1107/S1600536811010002
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AT nithinchandra 23dibromo34bromophenyl134methoxyphenylsydnon4ylpropan1one
AT kallurayabalakrishna 23dibromo34bromophenyl134methoxyphenylsydnon4ylpropan1one

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