Cargando…

3-(3-Amino­phenyl­sulfon­yl)aniline

In the title compound, C(12)H(12)N(2)O(2)S, the aromatic rings are oriented at a dihedral angle of 79.48 (4)°. Intra­molecular C—H⋯O hydrogen bonds result in the formation of two five-membered rings with envelope conformations. In the crystal structure, inter­molecular N—H⋯O hydrogen bonds link the...

Descripción completa

Detalles Bibliográficos
Autores principales: Ghazisaeidi, Reza, Yousefi, Mohammad
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968256/
https://www.ncbi.nlm.nih.gov/pubmed/21581840
http://dx.doi.org/10.1107/S1600536808043389
_version_ 1782189820456468480
author Ghazisaeidi, Reza
Yousefi, Mohammad
author_facet Ghazisaeidi, Reza
Yousefi, Mohammad
author_sort Ghazisaeidi, Reza
collection PubMed
description In the title compound, C(12)H(12)N(2)O(2)S, the aromatic rings are oriented at a dihedral angle of 79.48 (4)°. Intra­molecular C—H⋯O hydrogen bonds result in the formation of two five-membered rings with envelope conformations. In the crystal structure, inter­molecular N—H⋯O hydrogen bonds link the mol­ecules. π–π Contacts between the benzene rings, [centroid–centroid distance = 4.211 (3) Å] may further stabilize the structure.
format Text
id pubmed-2968256
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29682562010-12-30 3-(3-Amino­phenyl­sulfon­yl)aniline Ghazisaeidi, Reza Yousefi, Mohammad Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(12)H(12)N(2)O(2)S, the aromatic rings are oriented at a dihedral angle of 79.48 (4)°. Intra­molecular C—H⋯O hydrogen bonds result in the formation of two five-membered rings with envelope conformations. In the crystal structure, inter­molecular N—H⋯O hydrogen bonds link the mol­ecules. π–π Contacts between the benzene rings, [centroid–centroid distance = 4.211 (3) Å] may further stabilize the structure. International Union of Crystallography 2009-01-08 /pmc/articles/PMC2968256/ /pubmed/21581840 http://dx.doi.org/10.1107/S1600536808043389 Text en © Ghazisaeidi and Yousefi 2009 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
Ghazisaeidi, Reza
Yousefi, Mohammad
3-(3-Amino­phenyl­sulfon­yl)aniline
title 3-(3-Amino­phenyl­sulfon­yl)aniline
title_full 3-(3-Amino­phenyl­sulfon­yl)aniline
title_fullStr 3-(3-Amino­phenyl­sulfon­yl)aniline
title_full_unstemmed 3-(3-Amino­phenyl­sulfon­yl)aniline
title_short 3-(3-Amino­phenyl­sulfon­yl)aniline
title_sort 3-(3-amino­phenyl­sulfon­yl)aniline
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968256/
https://www.ncbi.nlm.nih.gov/pubmed/21581840
http://dx.doi.org/10.1107/S1600536808043389
work_keys_str_mv AT ghazisaeidireza 33aminophenylsulfonylaniline
AT yousefimohammad 33aminophenylsulfonylaniline