trans-5-(4-Chloro­phen­yl)-N-cyclo­hexyl-4-methyl-2-oxo-1,3-thia­zolidine-3-carboxamide

The title pesticide, C(17)H(21)ClN(2)O(2)S, has a trans arrangement of the 4-chloro­phenyl and 4-methyl substituents of the thia­zolidine ring; the structure features an intra­molecular amide–ring carbonyl N—H⋯O hydrogen bond. The thia­zolidine ring is almost planar, the largest deviation being 0.19...

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Detalles Bibliográficos
Autores principales: Yu, Ying-Hui, Liu, Ji-Long, Niu, Li-Zhong, Hou, Guang-Feng, Gao, Jin-Sheng
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961588/
https://www.ncbi.nlm.nih.gov/pubmed/21202544
http://dx.doi.org/10.1107/S1600536808012634
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author Yu, Ying-Hui
Liu, Ji-Long
Niu, Li-Zhong
Hou, Guang-Feng
Gao, Jin-Sheng
author_facet Yu, Ying-Hui
Liu, Ji-Long
Niu, Li-Zhong
Hou, Guang-Feng
Gao, Jin-Sheng
author_sort Yu, Ying-Hui
collection PubMed
description The title pesticide, C(17)H(21)ClN(2)O(2)S, has a trans arrangement of the 4-chloro­phenyl and 4-methyl substituents of the thia­zolidine ring; the structure features an intra­molecular amide–ring carbonyl N—H⋯O hydrogen bond. The thia­zolidine ring is almost planar, the largest deviation being 0.199 (1) Å for the methyl-substitued C atom, and the cyclohexane ring has a chair conformation.
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spelling pubmed-29615882010-12-30 trans-5-(4-Chloro­phen­yl)-N-cyclo­hexyl-4-methyl-2-oxo-1,3-thia­zolidine-3-carboxamide Yu, Ying-Hui Liu, Ji-Long Niu, Li-Zhong Hou, Guang-Feng Gao, Jin-Sheng Acta Crystallogr Sect E Struct Rep Online Organic Papers The title pesticide, C(17)H(21)ClN(2)O(2)S, has a trans arrangement of the 4-chloro­phenyl and 4-methyl substituents of the thia­zolidine ring; the structure features an intra­molecular amide–ring carbonyl N—H⋯O hydrogen bond. The thia­zolidine ring is almost planar, the largest deviation being 0.199 (1) Å for the methyl-substitued C atom, and the cyclohexane ring has a chair conformation. International Union of Crystallography 2008-05-07 /pmc/articles/PMC2961588/ /pubmed/21202544 http://dx.doi.org/10.1107/S1600536808012634 Text en © Yu et al. 2008 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
Yu, Ying-Hui
Liu, Ji-Long
Niu, Li-Zhong
Hou, Guang-Feng
Gao, Jin-Sheng
trans-5-(4-Chloro­phen­yl)-N-cyclo­hexyl-4-methyl-2-oxo-1,3-thia­zolidine-3-carboxamide
title trans-5-(4-Chloro­phen­yl)-N-cyclo­hexyl-4-methyl-2-oxo-1,3-thia­zolidine-3-carboxamide
title_full trans-5-(4-Chloro­phen­yl)-N-cyclo­hexyl-4-methyl-2-oxo-1,3-thia­zolidine-3-carboxamide
title_fullStr trans-5-(4-Chloro­phen­yl)-N-cyclo­hexyl-4-methyl-2-oxo-1,3-thia­zolidine-3-carboxamide
title_full_unstemmed trans-5-(4-Chloro­phen­yl)-N-cyclo­hexyl-4-methyl-2-oxo-1,3-thia­zolidine-3-carboxamide
title_short trans-5-(4-Chloro­phen­yl)-N-cyclo­hexyl-4-methyl-2-oxo-1,3-thia­zolidine-3-carboxamide
title_sort trans-5-(4-chloro­phen­yl)-n-cyclo­hexyl-4-methyl-2-oxo-1,3-thia­zolidine-3-carboxamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961588/
https://www.ncbi.nlm.nih.gov/pubmed/21202544
http://dx.doi.org/10.1107/S1600536808012634
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AT houguangfeng trans54chlorophenylncyclohexyl4methyl2oxo13thiazolidine3carboxamide
AT gaojinsheng trans54chlorophenylncyclohexyl4methyl2oxo13thiazolidine3carboxamide

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