(±)-1,2-Bis(N′-benzoyl­thio­ureido)cyclo­hexa­ne

In the title compound, C(22)H(24)N(4)O(2)S(2), the two thio­urea segments of the side-arm groups are inclined at a dihedral angle of 73.09 (9)°. The central cyclo­hexane bridge adopts a chair conformation. The mol­ecule is stabilized by N—H⋯O intra­molecular hydrogen bonds forming S(6) rings, and N—...

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Detalles Bibliográficos
Autores principales: Jumal, Juliana, Ibrahim, Abdul Razak, Yamin, Bohari M.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089146/
https://www.ncbi.nlm.nih.gov/pubmed/21754546
http://dx.doi.org/10.1107/S1600536811014991
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author Jumal, Juliana
Ibrahim, Abdul Razak
Yamin, Bohari M.
author_facet Jumal, Juliana
Ibrahim, Abdul Razak
Yamin, Bohari M.
author_sort Jumal, Juliana
collection PubMed
description In the title compound, C(22)H(24)N(4)O(2)S(2), the two thio­urea segments of the side-arm groups are inclined at a dihedral angle of 73.09 (9)°. The central cyclo­hexane bridge adopts a chair conformation. The mol­ecule is stabilized by N—H⋯O intra­molecular hydrogen bonds forming S(6) rings, and N—H⋯O and N—H⋯S inter­molecular hydrogen bonds forming infinite chains developing parallel to the b axis.
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spelling pubmed-30891462011-07-13 (±)-1,2-Bis(N′-benzoyl­thio­ureido)cyclo­hexa­ne Jumal, Juliana Ibrahim, Abdul Razak Yamin, Bohari M. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(22)H(24)N(4)O(2)S(2), the two thio­urea segments of the side-arm groups are inclined at a dihedral angle of 73.09 (9)°. The central cyclo­hexane bridge adopts a chair conformation. The mol­ecule is stabilized by N—H⋯O intra­molecular hydrogen bonds forming S(6) rings, and N—H⋯O and N—H⋯S inter­molecular hydrogen bonds forming infinite chains developing parallel to the b axis. International Union of Crystallography 2011-04-29 /pmc/articles/PMC3089146/ /pubmed/21754546 http://dx.doi.org/10.1107/S1600536811014991 Text en © Jumal 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
Jumal, Juliana
Ibrahim, Abdul Razak
Yamin, Bohari M.
(±)-1,2-Bis(N′-benzoyl­thio­ureido)cyclo­hexa­ne
title (±)-1,2-Bis(N′-benzoyl­thio­ureido)cyclo­hexa­ne
title_full (±)-1,2-Bis(N′-benzoyl­thio­ureido)cyclo­hexa­ne
title_fullStr (±)-1,2-Bis(N′-benzoyl­thio­ureido)cyclo­hexa­ne
title_full_unstemmed (±)-1,2-Bis(N′-benzoyl­thio­ureido)cyclo­hexa­ne
title_short (±)-1,2-Bis(N′-benzoyl­thio­ureido)cyclo­hexa­ne
title_sort (±)-1,2-bis(n′-benzoyl­thio­ureido)cyclo­hexa­ne
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089146/
https://www.ncbi.nlm.nih.gov/pubmed/21754546
http://dx.doi.org/10.1107/S1600536811014991
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