Cargando…
N,N′-Bis(3-chlorophenyl)succinamide
The complete molecule of the title compound, C(16)H(14)Cl(2)N(2)O(2), is generated by crystallographic inversion symmetry. The dihedral angle between the benzene ring and the NH—C(O)—C fragment is 32.8 (1)°. In the crystal, the molecules are linked by N—H⋯O hydrogen bonds into [100] chains....
Autores principales: | , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3099800/ https://www.ncbi.nlm.nih.gov/pubmed/21754229 http://dx.doi.org/10.1107/S1600536811010440 |
_version_ | 1782204087666737152 |
---|---|
author | Saraswathi, B. S. Foro, Sabine Gowda, B. Thimme |
author_facet | Saraswathi, B. S. Foro, Sabine Gowda, B. Thimme |
author_sort | Saraswathi, B. S. |
collection | PubMed |
description | The complete molecule of the title compound, C(16)H(14)Cl(2)N(2)O(2), is generated by crystallographic inversion symmetry. The dihedral angle between the benzene ring and the NH—C(O)—C fragment is 32.8 (1)°. In the crystal, the molecules are linked by N—H⋯O hydrogen bonds into [100] chains. |
format | Text |
id | pubmed-3099800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30998002011-07-13 N,N′-Bis(3-chlorophenyl)succinamide Saraswathi, B. S. Foro, Sabine Gowda, B. Thimme Acta Crystallogr Sect E Struct Rep Online Organic Papers The complete molecule of the title compound, C(16)H(14)Cl(2)N(2)O(2), is generated by crystallographic inversion symmetry. The dihedral angle between the benzene ring and the NH—C(O)—C fragment is 32.8 (1)°. In the crystal, the molecules are linked by N—H⋯O hydrogen bonds into [100] chains. International Union of Crystallography 2011-03-26 /pmc/articles/PMC3099800/ /pubmed/21754229 http://dx.doi.org/10.1107/S1600536811010440 Text en © Saraswathi et al. 2011 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 Saraswathi, B. S. Foro, Sabine Gowda, B. Thimme N,N′-Bis(3-chlorophenyl)succinamide |
title |
N,N′-Bis(3-chlorophenyl)succinamide |
title_full |
N,N′-Bis(3-chlorophenyl)succinamide |
title_fullStr |
N,N′-Bis(3-chlorophenyl)succinamide |
title_full_unstemmed |
N,N′-Bis(3-chlorophenyl)succinamide |
title_short |
N,N′-Bis(3-chlorophenyl)succinamide |
title_sort | n,n′-bis(3-chlorophenyl)succinamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3099800/ https://www.ncbi.nlm.nih.gov/pubmed/21754229 http://dx.doi.org/10.1107/S1600536811010440 |
work_keys_str_mv | AT saraswathibs nnbis3chlorophenylsuccinamide AT forosabine nnbis3chlorophenylsuccinamide AT gowdabthimme nnbis3chlorophenylsuccinamide |