N-(2-Oxo-2H-chromen-3-yl)benzamide

The phenyl ring in title mol­ecule, C(16)H(11)NO(3), forms a dihedral angle of 7.69 (6)° with the fused ring system. The observed conformation is stabilized by intra­molecular N—H⋯O and C—H⋯O inter­actions. In the crystal, supra­molecular chains are formed along the b axis which are mediated by π–π...

Descripción completa

Detalles Bibliográficos
Autores principales: Jotani, Mukesh M., Baldaniya, Bharat B., Tiekink, Edward R. T.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983879/
https://www.ncbi.nlm.nih.gov/pubmed/21580620
http://dx.doi.org/10.1107/S1600536810008275
_version_ 1782191980443336704
author Jotani, Mukesh M.
Baldaniya, Bharat B.
Tiekink, Edward R. T.
author_facet Jotani, Mukesh M.
Baldaniya, Bharat B.
Tiekink, Edward R. T.
author_sort Jotani, Mukesh M.
collection PubMed
description The phenyl ring in title mol­ecule, C(16)H(11)NO(3), forms a dihedral angle of 7.69 (6)° with the fused ring system. The observed conformation is stabilized by intra­molecular N—H⋯O and C—H⋯O inter­actions. In the crystal, supra­molecular chains are formed along the b axis which are mediated by π–π inter­actions [centroid–centroid distance = 3.614 (2) Å].
format Text
id pubmed-2983879
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29838792010-12-30 N-(2-Oxo-2H-chromen-3-yl)benzamide Jotani, Mukesh M. Baldaniya, Bharat B. Tiekink, Edward R. T. Acta Crystallogr Sect E Struct Rep Online Organic Papers The phenyl ring in title mol­ecule, C(16)H(11)NO(3), forms a dihedral angle of 7.69 (6)° with the fused ring system. The observed conformation is stabilized by intra­molecular N—H⋯O and C—H⋯O inter­actions. In the crystal, supra­molecular chains are formed along the b axis which are mediated by π–π inter­actions [centroid–centroid distance = 3.614 (2) Å]. International Union of Crystallography 2010-03-06 /pmc/articles/PMC2983879/ /pubmed/21580620 http://dx.doi.org/10.1107/S1600536810008275 Text en © Jotani 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
Jotani, Mukesh M.
Baldaniya, Bharat B.
Tiekink, Edward R. T.
N-(2-Oxo-2H-chromen-3-yl)benzamide
title N-(2-Oxo-2H-chromen-3-yl)benzamide
title_full N-(2-Oxo-2H-chromen-3-yl)benzamide
title_fullStr N-(2-Oxo-2H-chromen-3-yl)benzamide
title_full_unstemmed N-(2-Oxo-2H-chromen-3-yl)benzamide
title_short N-(2-Oxo-2H-chromen-3-yl)benzamide
title_sort n-(2-oxo-2h-chromen-3-yl)benzamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983879/
https://www.ncbi.nlm.nih.gov/pubmed/21580620
http://dx.doi.org/10.1107/S1600536810008275
work_keys_str_mv AT jotanimukeshm n2oxo2hchromen3ylbenzamide
AT baldaniyabharatb n2oxo2hchromen3ylbenzamide
AT tiekinkedwardrt n2oxo2hchromen3ylbenzamide

Ejemplares similares