Cargando…

2-(4-Chloro­phen­yl)-3-p-tolyl-1,3-thia­zolidin-4-one

The title compound, C(16)H(14)ClNOS, a potent anti­bacterial chemical, features a dihedral angle of 49.4 (1)° between the 4-tolyl and thia­zolidinone rings, and a dihedral angle of 87.2 (5)° between the thia­zolidinone and 4-chloro­phenyl rings.

Detalles Bibliográficos
Autores principales: Sun, Xiao-Jun, Zhou, Jian-Feng, Zhang, Zai-Chao, Wang, Yu-Jie
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969045/
https://www.ncbi.nlm.nih.gov/pubmed/21582585
http://dx.doi.org/10.1107/S1600536809010307
_version_ 1782190048128532480
author Sun, Xiao-Jun
Zhou, Jian-Feng
Zhang, Zai-Chao
Wang, Yu-Jie
author_facet Sun, Xiao-Jun
Zhou, Jian-Feng
Zhang, Zai-Chao
Wang, Yu-Jie
author_sort Sun, Xiao-Jun
collection PubMed
description The title compound, C(16)H(14)ClNOS, a potent anti­bacterial chemical, features a dihedral angle of 49.4 (1)° between the 4-tolyl and thia­zolidinone rings, and a dihedral angle of 87.2 (5)° between the thia­zolidinone and 4-chloro­phenyl rings.
format Text
id pubmed-2969045
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29690452010-12-30 2-(4-Chloro­phen­yl)-3-p-tolyl-1,3-thia­zolidin-4-one Sun, Xiao-Jun Zhou, Jian-Feng Zhang, Zai-Chao Wang, Yu-Jie Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(16)H(14)ClNOS, a potent anti­bacterial chemical, features a dihedral angle of 49.4 (1)° between the 4-tolyl and thia­zolidinone rings, and a dihedral angle of 87.2 (5)° between the thia­zolidinone and 4-chloro­phenyl rings. International Union of Crystallography 2009-03-25 /pmc/articles/PMC2969045/ /pubmed/21582585 http://dx.doi.org/10.1107/S1600536809010307 Text en © Sun et al. 2009 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
Sun, Xiao-Jun
Zhou, Jian-Feng
Zhang, Zai-Chao
Wang, Yu-Jie
2-(4-Chloro­phen­yl)-3-p-tolyl-1,3-thia­zolidin-4-one
title 2-(4-Chloro­phen­yl)-3-p-tolyl-1,3-thia­zolidin-4-one
title_full 2-(4-Chloro­phen­yl)-3-p-tolyl-1,3-thia­zolidin-4-one
title_fullStr 2-(4-Chloro­phen­yl)-3-p-tolyl-1,3-thia­zolidin-4-one
title_full_unstemmed 2-(4-Chloro­phen­yl)-3-p-tolyl-1,3-thia­zolidin-4-one
title_short 2-(4-Chloro­phen­yl)-3-p-tolyl-1,3-thia­zolidin-4-one
title_sort 2-(4-chloro­phen­yl)-3-p-tolyl-1,3-thia­zolidin-4-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969045/
https://www.ncbi.nlm.nih.gov/pubmed/21582585
http://dx.doi.org/10.1107/S1600536809010307
work_keys_str_mv AT sunxiaojun 24chlorophenyl3ptolyl13thiazolidin4one
AT zhoujianfeng 24chlorophenyl3ptolyl13thiazolidin4one
AT zhangzaichao 24chlorophenyl3ptolyl13thiazolidin4one
AT wangyujie 24chlorophenyl3ptolyl13thiazolidin4one