Cinnamoyl­thio­urea

In the title compound [systematic name: 1-(3-phenyl­prop-2-eno­yl)thio­urea], C(10)H(10)N(2)OS, the acetyl­thio­urea fragment and the phenyl ring adopt an E configuration. The roughly planar but-2-enoyl­thio­urea fragment [maximum deviation = 0.053 (3) Å] forms a dihedral of 10.54 (11)° with the phe...

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Detalles Bibliográficos
Autores principales: Hassan, Ibrahim N., Yamin, Bohari M., Kassim, Mohammad B.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009376/
https://www.ncbi.nlm.nih.gov/pubmed/21588993
http://dx.doi.org/10.1107/S1600536810040018
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author Hassan, Ibrahim N.
Yamin, Bohari M.
Kassim, Mohammad B.
author_facet Hassan, Ibrahim N.
Yamin, Bohari M.
Kassim, Mohammad B.
author_sort Hassan, Ibrahim N.
collection PubMed
description In the title compound [systematic name: 1-(3-phenyl­prop-2-eno­yl)thio­urea], C(10)H(10)N(2)OS, the acetyl­thio­urea fragment and the phenyl ring adopt an E configuration. The roughly planar but-2-enoyl­thio­urea fragment [maximum deviation = 0.053 (3) Å] forms a dihedral of 10.54 (11)° with the phenyl ring. An intra­molecular N—H⋯O hydrogen bond generates an S(6) ring. In the crystal, mol­ecules are linked into sheets parallel to (100) by N—H⋯S hydrogen bonds.
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spelling pubmed-30093762010-12-30 Cinnamoyl­thio­urea Hassan, Ibrahim N. Yamin, Bohari M. Kassim, Mohammad B. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound [systematic name: 1-(3-phenyl­prop-2-eno­yl)thio­urea], C(10)H(10)N(2)OS, the acetyl­thio­urea fragment and the phenyl ring adopt an E configuration. The roughly planar but-2-enoyl­thio­urea fragment [maximum deviation = 0.053 (3) Å] forms a dihedral of 10.54 (11)° with the phenyl ring. An intra­molecular N—H⋯O hydrogen bond generates an S(6) ring. In the crystal, mol­ecules are linked into sheets parallel to (100) by N—H⋯S hydrogen bonds. International Union of Crystallography 2010-10-13 /pmc/articles/PMC3009376/ /pubmed/21588993 http://dx.doi.org/10.1107/S1600536810040018 Text en © Hassan 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
Hassan, Ibrahim N.
Yamin, Bohari M.
Kassim, Mohammad B.
Cinnamoyl­thio­urea
title Cinnamoyl­thio­urea
title_full Cinnamoyl­thio­urea
title_fullStr Cinnamoyl­thio­urea
title_full_unstemmed Cinnamoyl­thio­urea
title_short Cinnamoyl­thio­urea
title_sort cinnamoyl­thio­urea
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009376/
https://www.ncbi.nlm.nih.gov/pubmed/21588993
http://dx.doi.org/10.1107/S1600536810040018
work_keys_str_mv AT hassanibrahimn cinnamoylthiourea
AT yaminboharim cinnamoylthiourea
AT kassimmohammadb cinnamoylthiourea

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