(E)-1-Bromo-4-(2-nitro­prop-1-en­yl)benzene

The title compound, C(9)H(8)BrNO(2), which was synthesized by the condensation of 4-bromo­benzaldehyde with nitro­ethane, possesses a trans configuration. The dihedral angle between the benzene ring and the mean plane of the double bond is 7.31 (3)°. The crystal structure is stabilized by short inte...

Descripción completa

Detalles Bibliográficos
Autor principal: Li, Bailin
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971981/
https://www.ncbi.nlm.nih.gov/pubmed/21578889
http://dx.doi.org/10.1107/S1600536809048910
_version_ 1782190715693957120
author Li, Bailin
author_facet Li, Bailin
author_sort Li, Bailin
collection PubMed
description The title compound, C(9)H(8)BrNO(2), which was synthesized by the condensation of 4-bromo­benzaldehyde with nitro­ethane, possesses a trans configuration. The dihedral angle between the benzene ring and the mean plane of the double bond is 7.31 (3)°. The crystal structure is stabilized by short inter­molecular Br⋯O contacts [3.168 (4) Å].
format Text
id pubmed-2971981
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29719812010-12-30 (E)-1-Bromo-4-(2-nitro­prop-1-en­yl)benzene Li, Bailin Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(9)H(8)BrNO(2), which was synthesized by the condensation of 4-bromo­benzaldehyde with nitro­ethane, possesses a trans configuration. The dihedral angle between the benzene ring and the mean plane of the double bond is 7.31 (3)°. The crystal structure is stabilized by short inter­molecular Br⋯O contacts [3.168 (4) Å]. International Union of Crystallography 2009-11-21 /pmc/articles/PMC2971981/ /pubmed/21578889 http://dx.doi.org/10.1107/S1600536809048910 Text en © Bailin Li 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
Li, Bailin
(E)-1-Bromo-4-(2-nitro­prop-1-en­yl)benzene
title (E)-1-Bromo-4-(2-nitro­prop-1-en­yl)benzene
title_full (E)-1-Bromo-4-(2-nitro­prop-1-en­yl)benzene
title_fullStr (E)-1-Bromo-4-(2-nitro­prop-1-en­yl)benzene
title_full_unstemmed (E)-1-Bromo-4-(2-nitro­prop-1-en­yl)benzene
title_short (E)-1-Bromo-4-(2-nitro­prop-1-en­yl)benzene
title_sort (e)-1-bromo-4-(2-nitro­prop-1-en­yl)benzene
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971981/
https://www.ncbi.nlm.nih.gov/pubmed/21578889
http://dx.doi.org/10.1107/S1600536809048910
work_keys_str_mv AT libailin e1bromo42nitroprop1enylbenzene

Ejemplares similares