2-Bromo­pyridine-3-carboxylic acid

The carboxylic acid residue in the title compound, C(6)H(4)BrNO(2), is twisted out of the plane of the other atoms, as indicated by the (Br)C—C—C—O(carbon­yl) torsion angle of −20.1 (9)°. In the crystal, supra­molecular chains mediated by O—H⋯N hydrogen bonds are formed with base vector [201] and C—...

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Detalles Bibliográficos
Autores principales: Howie, R. Alan, Gonçalves, Raoni S., de Souza, Marcus V. N., Tiekink, Edward R. T., Wardell, James L.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979810/
https://www.ncbi.nlm.nih.gov/pubmed/21579893
http://dx.doi.org/10.1107/S1600536810003314
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author Howie, R. Alan
Gonçalves, Raoni S.
de Souza, Marcus V. N.
Tiekink, Edward R. T.
Wardell, James L.
author_facet Howie, R. Alan
Gonçalves, Raoni S.
de Souza, Marcus V. N.
Tiekink, Edward R. T.
Wardell, James L.
author_sort Howie, R. Alan
collection PubMed
description The carboxylic acid residue in the title compound, C(6)H(4)BrNO(2), is twisted out of the plane of the other atoms, as indicated by the (Br)C—C—C—O(carbon­yl) torsion angle of −20.1 (9)°. In the crystal, supra­molecular chains mediated by O—H⋯N hydrogen bonds are formed with base vector [201] and C—H⋯O inter­actions reinforce the packing.
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spelling pubmed-29798102010-12-30 2-Bromo­pyridine-3-carboxylic acid Howie, R. Alan Gonçalves, Raoni S. de Souza, Marcus V. N. Tiekink, Edward R. T. Wardell, James L. Acta Crystallogr Sect E Struct Rep Online Organic Papers The carboxylic acid residue in the title compound, C(6)H(4)BrNO(2), is twisted out of the plane of the other atoms, as indicated by the (Br)C—C—C—O(carbon­yl) torsion angle of −20.1 (9)°. In the crystal, supra­molecular chains mediated by O—H⋯N hydrogen bonds are formed with base vector [201] and C—H⋯O inter­actions reinforce the packing. International Union of Crystallography 2010-01-30 /pmc/articles/PMC2979810/ /pubmed/21579893 http://dx.doi.org/10.1107/S1600536810003314 Text en © Howie 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
Howie, R. Alan
Gonçalves, Raoni S.
de Souza, Marcus V. N.
Tiekink, Edward R. T.
Wardell, James L.
2-Bromo­pyridine-3-carboxylic acid
title 2-Bromo­pyridine-3-carboxylic acid
title_full 2-Bromo­pyridine-3-carboxylic acid
title_fullStr 2-Bromo­pyridine-3-carboxylic acid
title_full_unstemmed 2-Bromo­pyridine-3-carboxylic acid
title_short 2-Bromo­pyridine-3-carboxylic acid
title_sort 2-bromo­pyridine-3-carboxylic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979810/
https://www.ncbi.nlm.nih.gov/pubmed/21579893
http://dx.doi.org/10.1107/S1600536810003314
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AT tiekinkedwardrt 2bromopyridine3carboxylicacid
AT wardelljamesl 2bromopyridine3carboxylicacid

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