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1,3-Bis(bromomethyl)-2-nitrobenzene
In the title compound, C(8)H(7)Br(2)NO(2), an intermediate for the synthesis of macrocycles, the NO(2) group makes a dihedral angle of 65.07 (19)° with the arene ring, and the bromomethyl substituents adopt a trans conformation about the ring such that the molecule closely approximates C2 symmetr...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2984041/ https://www.ncbi.nlm.nih.gov/pubmed/21580661 http://dx.doi.org/10.1107/S160053681000718X |
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author | Arshad, Muhammad Nadeem Edson, Katheryne Zumberge Mough, Scott T. Holman, K. Travis |
author_facet | Arshad, Muhammad Nadeem Edson, Katheryne Zumberge Mough, Scott T. Holman, K. Travis |
author_sort | Arshad, Muhammad Nadeem |
collection | PubMed |
description | In the title compound, C(8)H(7)Br(2)NO(2), an intermediate for the synthesis of macrocycles, the NO(2) group makes a dihedral angle of 65.07 (19)° with the arene ring, and the bromomethyl substituents adopt a trans conformation about the ring such that the molecule closely approximates C2 symmetry. |
format | Text |
id | pubmed-2984041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29840412010-12-30 1,3-Bis(bromomethyl)-2-nitrobenzene Arshad, Muhammad Nadeem Edson, Katheryne Zumberge Mough, Scott T. Holman, K. Travis Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(8)H(7)Br(2)NO(2), an intermediate for the synthesis of macrocycles, the NO(2) group makes a dihedral angle of 65.07 (19)° with the arene ring, and the bromomethyl substituents adopt a trans conformation about the ring such that the molecule closely approximates C2 symmetry. International Union of Crystallography 2010-03-13 /pmc/articles/PMC2984041/ /pubmed/21580661 http://dx.doi.org/10.1107/S160053681000718X Text en © Arshad 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 Arshad, Muhammad Nadeem Edson, Katheryne Zumberge Mough, Scott T. Holman, K. Travis 1,3-Bis(bromomethyl)-2-nitrobenzene |
title | 1,3-Bis(bromomethyl)-2-nitrobenzene |
title_full | 1,3-Bis(bromomethyl)-2-nitrobenzene |
title_fullStr | 1,3-Bis(bromomethyl)-2-nitrobenzene |
title_full_unstemmed | 1,3-Bis(bromomethyl)-2-nitrobenzene |
title_short | 1,3-Bis(bromomethyl)-2-nitrobenzene |
title_sort | 1,3-bis(bromomethyl)-2-nitrobenzene |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2984041/ https://www.ncbi.nlm.nih.gov/pubmed/21580661 http://dx.doi.org/10.1107/S160053681000718X |
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