Dimethyl 2-amino­biphenyl-4,4′-di­carboxyl­ate

The title compound, C(16)H(15)NO(4), exhibits two near-planar aromatic ester groups with a maximum aryl–ester torsion angle of 1.9 (2)°. The dihedral angle between the benzene rings is 44.7 (1)°. In the crystal, N—H⋯O hydrogen bonding is observed along with C—H⋯O contacts, forming chanins along [101...

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Detalles Bibliográficos
Autores principales: Lehane, Ryan L., Golen, James A., Rheingold, Arnold L., Manke, David R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648318/
https://www.ncbi.nlm.nih.gov/pubmed/23723938
http://dx.doi.org/10.1107/S1600536813010775
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author Lehane, Ryan L.
Golen, James A.
Rheingold, Arnold L.
Manke, David R.
author_facet Lehane, Ryan L.
Golen, James A.
Rheingold, Arnold L.
Manke, David R.
author_sort Lehane, Ryan L.
collection PubMed
description The title compound, C(16)H(15)NO(4), exhibits two near-planar aromatic ester groups with a maximum aryl–ester torsion angle of 1.9 (2)°. The dihedral angle between the benzene rings is 44.7 (1)°. In the crystal, N—H⋯O hydrogen bonding is observed along with C—H⋯O contacts, forming chanins along [101]. No π–π inter­actions were noted between the benzene rings.
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spelling pubmed-36483182013-05-30 Dimethyl 2-amino­biphenyl-4,4′-di­carboxyl­ate Lehane, Ryan L. Golen, James A. Rheingold, Arnold L. Manke, David R. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(16)H(15)NO(4), exhibits two near-planar aromatic ester groups with a maximum aryl–ester torsion angle of 1.9 (2)°. The dihedral angle between the benzene rings is 44.7 (1)°. In the crystal, N—H⋯O hydrogen bonding is observed along with C—H⋯O contacts, forming chanins along [101]. No π–π inter­actions were noted between the benzene rings. International Union of Crystallography 2013-04-27 /pmc/articles/PMC3648318/ /pubmed/23723938 http://dx.doi.org/10.1107/S1600536813010775 Text en © Lehane et al. 2013 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
Lehane, Ryan L.
Golen, James A.
Rheingold, Arnold L.
Manke, David R.
Dimethyl 2-amino­biphenyl-4,4′-di­carboxyl­ate
title Dimethyl 2-amino­biphenyl-4,4′-di­carboxyl­ate
title_full Dimethyl 2-amino­biphenyl-4,4′-di­carboxyl­ate
title_fullStr Dimethyl 2-amino­biphenyl-4,4′-di­carboxyl­ate
title_full_unstemmed Dimethyl 2-amino­biphenyl-4,4′-di­carboxyl­ate
title_short Dimethyl 2-amino­biphenyl-4,4′-di­carboxyl­ate
title_sort dimethyl 2-amino­biphenyl-4,4′-di­carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648318/
https://www.ncbi.nlm.nih.gov/pubmed/23723938
http://dx.doi.org/10.1107/S1600536813010775
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AT mankedavidr dimethyl2aminobiphenyl44dicarboxylate

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