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Crystal structure of 4-cyclohexyl-1-(propan-2-ylidene)thiosemicarbazide
In the title compound, C(10)H(19)N(3)S, the cyclohexyl group adopts a chair conformation and adopts a position approximately syn to the thione S atom. The CN(2)S thiourea moiety makes dihedral angle of 13.13 (10)° with the propan-2-ylideneamino group. An intramolecular N—H⋯N hydrogen bond is no...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4257229/ https://www.ncbi.nlm.nih.gov/pubmed/25484699 http://dx.doi.org/10.1107/S160053681402025X |
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author | Yamin, Bohari M Rodis, Monica Lulo Chee, Dayang N. B. A |
author_facet | Yamin, Bohari M Rodis, Monica Lulo Chee, Dayang N. B. A |
author_sort | Yamin, Bohari M |
collection | PubMed |
description | In the title compound, C(10)H(19)N(3)S, the cyclohexyl group adopts a chair conformation and adopts a position approximately syn to the thione S atom. The CN(2)S thiourea moiety makes dihedral angle of 13.13 (10)° with the propan-2-ylideneamino group. An intramolecular N—H⋯N hydrogen bond is noted. In the crystal, inversion dimers linked by pairs of N—H⋯S hydrogen bonds generate R (2) (2)(8) loops. |
format | Online Article Text |
id | pubmed-4257229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-42572292014-12-05 Crystal structure of 4-cyclohexyl-1-(propan-2-ylidene)thiosemicarbazide Yamin, Bohari M Rodis, Monica Lulo Chee, Dayang N. B. A Acta Crystallogr Sect E Struct Rep Online Data Reports In the title compound, C(10)H(19)N(3)S, the cyclohexyl group adopts a chair conformation and adopts a position approximately syn to the thione S atom. The CN(2)S thiourea moiety makes dihedral angle of 13.13 (10)° with the propan-2-ylideneamino group. An intramolecular N—H⋯N hydrogen bond is noted. In the crystal, inversion dimers linked by pairs of N—H⋯S hydrogen bonds generate R (2) (2)(8) loops. International Union of Crystallography 2014-09-13 /pmc/articles/PMC4257229/ /pubmed/25484699 http://dx.doi.org/10.1107/S160053681402025X Text en © Yamin et al. 2014 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 | Data Reports Yamin, Bohari M Rodis, Monica Lulo Chee, Dayang N. B. A Crystal structure of 4-cyclohexyl-1-(propan-2-ylidene)thiosemicarbazide |
title | Crystal structure of 4-cyclohexyl-1-(propan-2-ylidene)thiosemicarbazide |
title_full | Crystal structure of 4-cyclohexyl-1-(propan-2-ylidene)thiosemicarbazide |
title_fullStr | Crystal structure of 4-cyclohexyl-1-(propan-2-ylidene)thiosemicarbazide |
title_full_unstemmed | Crystal structure of 4-cyclohexyl-1-(propan-2-ylidene)thiosemicarbazide |
title_short | Crystal structure of 4-cyclohexyl-1-(propan-2-ylidene)thiosemicarbazide |
title_sort | crystal structure of 4-cyclohexyl-1-(propan-2-ylidene)thiosemicarbazide |
topic | Data Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4257229/ https://www.ncbi.nlm.nih.gov/pubmed/25484699 http://dx.doi.org/10.1107/S160053681402025X |
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