3-({[(1-Phenyl­eth­yl)sulfan­yl]methane­thio­yl}sulfan­yl)propanoic acid

In the title compound, C(12)H(14)O(2)S(3), a chain transfer agent (CTA) used in polymerization, the dihedral angle between the aromatic ring and the CS(3) grouping is 84.20 (10)°. In the crystal, carb­oxy­lic acid inversion dimers linked by pairs of O—H⋯O hydrogen bonds generate R (2) (2)(8) loops....

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Detalles Bibliográficos
Autores principales: Kannan, M., Ramkumar, V., Dhamodharan, R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238997/
https://www.ncbi.nlm.nih.gov/pubmed/22199846
http://dx.doi.org/10.1107/S1600536811046873
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author Kannan, M.
Ramkumar, V.
Dhamodharan, R.
author_facet Kannan, M.
Ramkumar, V.
Dhamodharan, R.
author_sort Kannan, M.
collection PubMed
description In the title compound, C(12)H(14)O(2)S(3), a chain transfer agent (CTA) used in polymerization, the dihedral angle between the aromatic ring and the CS(3) grouping is 84.20 (10)°. In the crystal, carb­oxy­lic acid inversion dimers linked by pairs of O—H⋯O hydrogen bonds generate R (2) (2)(8) loops.
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spelling pubmed-32389972011-12-23 3-({[(1-Phenyl­eth­yl)sulfan­yl]methane­thio­yl}sulfan­yl)propanoic acid Kannan, M. Ramkumar, V. Dhamodharan, R. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(12)H(14)O(2)S(3), a chain transfer agent (CTA) used in polymerization, the dihedral angle between the aromatic ring and the CS(3) grouping is 84.20 (10)°. In the crystal, carb­oxy­lic acid inversion dimers linked by pairs of O—H⋯O hydrogen bonds generate R (2) (2)(8) loops. International Union of Crystallography 2011-11-19 /pmc/articles/PMC3238997/ /pubmed/22199846 http://dx.doi.org/10.1107/S1600536811046873 Text en © Kannan et al. 2011 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
Kannan, M.
Ramkumar, V.
Dhamodharan, R.
3-({[(1-Phenyl­eth­yl)sulfan­yl]methane­thio­yl}sulfan­yl)propanoic acid
title 3-({[(1-Phenyl­eth­yl)sulfan­yl]methane­thio­yl}sulfan­yl)propanoic acid
title_full 3-({[(1-Phenyl­eth­yl)sulfan­yl]methane­thio­yl}sulfan­yl)propanoic acid
title_fullStr 3-({[(1-Phenyl­eth­yl)sulfan­yl]methane­thio­yl}sulfan­yl)propanoic acid
title_full_unstemmed 3-({[(1-Phenyl­eth­yl)sulfan­yl]methane­thio­yl}sulfan­yl)propanoic acid
title_short 3-({[(1-Phenyl­eth­yl)sulfan­yl]methane­thio­yl}sulfan­yl)propanoic acid
title_sort 3-({[(1-phenyl­eth­yl)sulfan­yl]methane­thio­yl}sulfan­yl)propanoic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238997/
https://www.ncbi.nlm.nih.gov/pubmed/22199846
http://dx.doi.org/10.1107/S1600536811046873
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AT ramkumarv 31phenylethylsulfanylmethanethioylsulfanylpropanoicacid
AT dhamodharanr 31phenylethylsulfanylmethanethioylsulfanylpropanoicacid

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