2-Cyclo­hexyl­idene-N-methyl­hydrazine­carbothio­amide

The title compound C(8)H(15)N(3)S has two mol­ecules in the asymmetric unit in which cis–trans isomerism is exhibited around the N(NH)C=S bonds. The cyclo­hexyl rings in both mol­ecules adopt a chair conformation. In the crystal, N—H⋯S hydrogen bonding produces dimers, which are inter­connected thro...

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Detalles Bibliográficos
Autores principales: Tayamon, Shahedeh, Mazlan, Nurul Ain, Ravoof, Thahira Begum S. A., Mohamed Tahir, Mohamed Ibrahim, Crouse, Karen A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515211/
https://www.ncbi.nlm.nih.gov/pubmed/23284431
http://dx.doi.org/10.1107/S1600536812042018
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author Tayamon, Shahedeh
Mazlan, Nurul Ain
Ravoof, Thahira Begum S. A.
Mohamed Tahir, Mohamed Ibrahim
Crouse, Karen A
author_facet Tayamon, Shahedeh
Mazlan, Nurul Ain
Ravoof, Thahira Begum S. A.
Mohamed Tahir, Mohamed Ibrahim
Crouse, Karen A
author_sort Tayamon, Shahedeh
collection PubMed
description The title compound C(8)H(15)N(3)S has two mol­ecules in the asymmetric unit in which cis–trans isomerism is exhibited around the N(NH)C=S bonds. The cyclo­hexyl rings in both mol­ecules adopt a chair conformation. In the crystal, N—H⋯S hydrogen bonding produces dimers, which are inter­connected through further N—H⋯S hydrogen bonds, forming chains along the b-axis direction.
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spelling pubmed-35152112013-01-02 2-Cyclo­hexyl­idene-N-methyl­hydrazine­carbothio­amide Tayamon, Shahedeh Mazlan, Nurul Ain Ravoof, Thahira Begum S. A. Mohamed Tahir, Mohamed Ibrahim Crouse, Karen A Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound C(8)H(15)N(3)S has two mol­ecules in the asymmetric unit in which cis–trans isomerism is exhibited around the N(NH)C=S bonds. The cyclo­hexyl rings in both mol­ecules adopt a chair conformation. In the crystal, N—H⋯S hydrogen bonding produces dimers, which are inter­connected through further N—H⋯S hydrogen bonds, forming chains along the b-axis direction. International Union of Crystallography 2012-10-13 /pmc/articles/PMC3515211/ /pubmed/23284431 http://dx.doi.org/10.1107/S1600536812042018 Text en © Tayamon et al. 2012 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
Tayamon, Shahedeh
Mazlan, Nurul Ain
Ravoof, Thahira Begum S. A.
Mohamed Tahir, Mohamed Ibrahim
Crouse, Karen A
2-Cyclo­hexyl­idene-N-methyl­hydrazine­carbothio­amide
title 2-Cyclo­hexyl­idene-N-methyl­hydrazine­carbothio­amide
title_full 2-Cyclo­hexyl­idene-N-methyl­hydrazine­carbothio­amide
title_fullStr 2-Cyclo­hexyl­idene-N-methyl­hydrazine­carbothio­amide
title_full_unstemmed 2-Cyclo­hexyl­idene-N-methyl­hydrazine­carbothio­amide
title_short 2-Cyclo­hexyl­idene-N-methyl­hydrazine­carbothio­amide
title_sort 2-cyclo­hexyl­idene-n-methyl­hydrazine­carbothio­amide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515211/
https://www.ncbi.nlm.nih.gov/pubmed/23284431
http://dx.doi.org/10.1107/S1600536812042018
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AT ravoofthahirabegumsa 2cyclohexylidenenmethylhydrazinecarbothioamide
AT mohamedtahirmohamedibrahim 2cyclohexylidenenmethylhydrazinecarbothioamide
AT crousekarena 2cyclohexylidenenmethylhydrazinecarbothioamide

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