3-Butyl-2-phenyl-1,3-thia­zolidine-1,4-dione

In the title compound, C(13)H(17)NO(2)S, the thia­zolidine-1,4-dione ring adopts an envelope conformation with the S atom lying 0.631 (4) Å out of the plane formed by the other four ring atoms; the phenyl ring is almost perpendicular [88.74 (8)°] with respect to the ring C—C—N—C atoms and the butyl...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Qiang, Xu, Zhouqin, Sun, Yanchun
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979582/
https://www.ncbi.nlm.nih.gov/pubmed/21579498
http://dx.doi.org/10.1107/S1600536810018003
_version_ 1782191447520313344
author Wang, Qiang
Xu, Zhouqin
Sun, Yanchun
author_facet Wang, Qiang
Xu, Zhouqin
Sun, Yanchun
author_sort Wang, Qiang
collection PubMed
description In the title compound, C(13)H(17)NO(2)S, the thia­zolidine-1,4-dione ring adopts an envelope conformation with the S atom lying 0.631 (4) Å out of the plane formed by the other four ring atoms; the phenyl ring is almost perpendicular [88.74 (8)°] with respect to the ring C—C—N—C atoms and the butyl chain is in a fully extended conformation. In the crystal, a supra­molecular two-dimensional arrangement arises from weak inter­molecular C—H⋯O inter­actions.
format Text
id pubmed-2979582
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29795822010-12-30 3-Butyl-2-phenyl-1,3-thia­zolidine-1,4-dione Wang, Qiang Xu, Zhouqin Sun, Yanchun Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(17)NO(2)S, the thia­zolidine-1,4-dione ring adopts an envelope conformation with the S atom lying 0.631 (4) Å out of the plane formed by the other four ring atoms; the phenyl ring is almost perpendicular [88.74 (8)°] with respect to the ring C—C—N—C atoms and the butyl chain is in a fully extended conformation. In the crystal, a supra­molecular two-dimensional arrangement arises from weak inter­molecular C—H⋯O inter­actions. International Union of Crystallography 2010-05-22 /pmc/articles/PMC2979582/ /pubmed/21579498 http://dx.doi.org/10.1107/S1600536810018003 Text en © Wang 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
Wang, Qiang
Xu, Zhouqin
Sun, Yanchun
3-Butyl-2-phenyl-1,3-thia­zolidine-1,4-dione
title 3-Butyl-2-phenyl-1,3-thia­zolidine-1,4-dione
title_full 3-Butyl-2-phenyl-1,3-thia­zolidine-1,4-dione
title_fullStr 3-Butyl-2-phenyl-1,3-thia­zolidine-1,4-dione
title_full_unstemmed 3-Butyl-2-phenyl-1,3-thia­zolidine-1,4-dione
title_short 3-Butyl-2-phenyl-1,3-thia­zolidine-1,4-dione
title_sort 3-butyl-2-phenyl-1,3-thia­zolidine-1,4-dione
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979582/
https://www.ncbi.nlm.nih.gov/pubmed/21579498
http://dx.doi.org/10.1107/S1600536810018003
work_keys_str_mv AT wangqiang 3butyl2phenyl13thiazolidine14dione
AT xuzhouqin 3butyl2phenyl13thiazolidine14dione
AT sunyanchun 3butyl2phenyl13thiazolidine14dione

Ejemplares similares