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2-Amino-5-nitro­benzoic acid

In the title compound, C(7)H(6)N(2)O(4), an intra­molecular N—H⋯O hydrogen bond generates an S(6) ring. In the crystal, inversion dimers linked by pairs of O—H⋯O hydrogen bonds generate R (2) (2)(8) loops. Inter­molecular N—H⋯O and C—H⋯O hydrogen bonds then link the dimers, generating R (3) (3)(16)R...

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Detalles Bibliográficos
Autores principales: Odabaşoğlu, Hakkı Yasin, Büyükgüngör, Orhan, Avinç, Osman Ozan, Odabaşoğlu, Mustafa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275255/
https://www.ncbi.nlm.nih.gov/pubmed/22347111
http://dx.doi.org/10.1107/S1600536812002474
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author Odabaşoğlu, Hakkı Yasin
Büyükgüngör, Orhan
Avinç, Osman Ozan
Odabaşoğlu, Mustafa
author_facet Odabaşoğlu, Hakkı Yasin
Büyükgüngör, Orhan
Avinç, Osman Ozan
Odabaşoğlu, Mustafa
author_sort Odabaşoğlu, Hakkı Yasin
collection PubMed
description In the title compound, C(7)H(6)N(2)O(4), an intra­molecular N—H⋯O hydrogen bond generates an S(6) ring. In the crystal, inversion dimers linked by pairs of O—H⋯O hydrogen bonds generate R (2) (2)(8) loops. Inter­molecular N—H⋯O and C—H⋯O hydrogen bonds then link the dimers, generating R (3) (3)(16)R (2) (1)(6) motifs. The whole mol­ecule is essentially planar, with the greatest deviation from the mean plane being 0.065 (2) Å.
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spelling pubmed-32752552012-02-15 2-Amino-5-nitro­benzoic acid Odabaşoğlu, Hakkı Yasin Büyükgüngör, Orhan Avinç, Osman Ozan Odabaşoğlu, Mustafa Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(7)H(6)N(2)O(4), an intra­molecular N—H⋯O hydrogen bond generates an S(6) ring. In the crystal, inversion dimers linked by pairs of O—H⋯O hydrogen bonds generate R (2) (2)(8) loops. Inter­molecular N—H⋯O and C—H⋯O hydrogen bonds then link the dimers, generating R (3) (3)(16)R (2) (1)(6) motifs. The whole mol­ecule is essentially planar, with the greatest deviation from the mean plane being 0.065 (2) Å. International Union of Crystallography 2012-01-25 /pmc/articles/PMC3275255/ /pubmed/22347111 http://dx.doi.org/10.1107/S1600536812002474 Text en © Odabaşoğlu et al. 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
Odabaşoğlu, Hakkı Yasin
Büyükgüngör, Orhan
Avinç, Osman Ozan
Odabaşoğlu, Mustafa
2-Amino-5-nitro­benzoic acid
title 2-Amino-5-nitro­benzoic acid
title_full 2-Amino-5-nitro­benzoic acid
title_fullStr 2-Amino-5-nitro­benzoic acid
title_full_unstemmed 2-Amino-5-nitro­benzoic acid
title_short 2-Amino-5-nitro­benzoic acid
title_sort 2-amino-5-nitro­benzoic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275255/
https://www.ncbi.nlm.nih.gov/pubmed/22347111
http://dx.doi.org/10.1107/S1600536812002474
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