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3-Bromopyridin-2-amine
In the crystal structure of the title compound, C(5)H(5)BrN(2), molecules assemble via pairs of N—H⋯N hydrogen bonds into inversion dimers using only the syn H atom on the amine group. These dimers then assemble further into two-dimensional layers via type I C—Br⋯Br [Br⋯Br = 3.693 (s6) Å] halogen b...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275062/ https://www.ncbi.nlm.nih.gov/pubmed/22347007 http://dx.doi.org/10.1107/S1600536811055541 |
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author | Johnson, Marcelle Lemmerer, Andreas |
author_facet | Johnson, Marcelle Lemmerer, Andreas |
author_sort | Johnson, Marcelle |
collection | PubMed |
description | In the crystal structure of the title compound, C(5)H(5)BrN(2), molecules assemble via pairs of N—H⋯N hydrogen bonds into inversion dimers using only the syn H atom on the amine group. These dimers then assemble further into two-dimensional layers via type I C—Br⋯Br [Br⋯Br = 3.693 (s6) Å] halogen bonding along the (102) plane. |
format | Online Article Text |
id | pubmed-3275062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32750622012-02-15 3-Bromopyridin-2-amine Johnson, Marcelle Lemmerer, Andreas Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(5)H(5)BrN(2), molecules assemble via pairs of N—H⋯N hydrogen bonds into inversion dimers using only the syn H atom on the amine group. These dimers then assemble further into two-dimensional layers via type I C—Br⋯Br [Br⋯Br = 3.693 (s6) Å] halogen bonding along the (102) plane. International Union of Crystallography 2012-01-14 /pmc/articles/PMC3275062/ /pubmed/22347007 http://dx.doi.org/10.1107/S1600536811055541 Text en © Johnson and Lemmerer 2012 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 Johnson, Marcelle Lemmerer, Andreas 3-Bromopyridin-2-amine |
title | 3-Bromopyridin-2-amine |
title_full | 3-Bromopyridin-2-amine |
title_fullStr | 3-Bromopyridin-2-amine |
title_full_unstemmed | 3-Bromopyridin-2-amine |
title_short | 3-Bromopyridin-2-amine |
title_sort | 3-bromopyridin-2-amine |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275062/ https://www.ncbi.nlm.nih.gov/pubmed/22347007 http://dx.doi.org/10.1107/S1600536811055541 |
work_keys_str_mv | AT johnsonmarcelle 3bromopyridin2amine AT lemmererandreas 3bromopyridin2amine |