N (2),N (2),N (5),N (5)-Tetra­kis(2-chloro­ethyl)-3,4-dimethyl­thio­phene-2,5-dicarboxamide

In the title compound, C(16)H(22)Cl(4)N(2)O(2)S, the two imide groups adopt a trans arrangement relative to the central thienyl ring, so the four terminal 2-chloro­ethyl arms adopt different orientations. In the crystal, mol­ecules are linked by weak C—H⋯Cl and C—H⋯O hydrogen bonds into a three-dime...

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Detalles Bibliográficos
Autores principales: Tang, Yi-Dan, Geng, Rong-Xia, Zhou, Cheng-He
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980083/
https://www.ncbi.nlm.nih.gov/pubmed/21579991
http://dx.doi.org/10.1107/S1600536809052374
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author Tang, Yi-Dan
Geng, Rong-Xia
Zhou, Cheng-He
author_facet Tang, Yi-Dan
Geng, Rong-Xia
Zhou, Cheng-He
author_sort Tang, Yi-Dan
collection PubMed
description In the title compound, C(16)H(22)Cl(4)N(2)O(2)S, the two imide groups adopt a trans arrangement relative to the central thienyl ring, so the four terminal 2-chloro­ethyl arms adopt different orientations. In the crystal, mol­ecules are linked by weak C—H⋯Cl and C—H⋯O hydrogen bonds into a three-dimensional network.
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spelling pubmed-29800832010-12-30 N (2),N (2),N (5),N (5)-Tetra­kis(2-chloro­ethyl)-3,4-dimethyl­thio­phene-2,5-dicarboxamide Tang, Yi-Dan Geng, Rong-Xia Zhou, Cheng-He Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(22)Cl(4)N(2)O(2)S, the two imide groups adopt a trans arrangement relative to the central thienyl ring, so the four terminal 2-chloro­ethyl arms adopt different orientations. In the crystal, mol­ecules are linked by weak C—H⋯Cl and C—H⋯O hydrogen bonds into a three-dimensional network. International Union of Crystallography 2009-12-12 /pmc/articles/PMC2980083/ /pubmed/21579991 http://dx.doi.org/10.1107/S1600536809052374 Text en © Tang 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
Tang, Yi-Dan
Geng, Rong-Xia
Zhou, Cheng-He
N (2),N (2),N (5),N (5)-Tetra­kis(2-chloro­ethyl)-3,4-dimethyl­thio­phene-2,5-dicarboxamide
title N (2),N (2),N (5),N (5)-Tetra­kis(2-chloro­ethyl)-3,4-dimethyl­thio­phene-2,5-dicarboxamide
title_full N (2),N (2),N (5),N (5)-Tetra­kis(2-chloro­ethyl)-3,4-dimethyl­thio­phene-2,5-dicarboxamide
title_fullStr N (2),N (2),N (5),N (5)-Tetra­kis(2-chloro­ethyl)-3,4-dimethyl­thio­phene-2,5-dicarboxamide
title_full_unstemmed N (2),N (2),N (5),N (5)-Tetra­kis(2-chloro­ethyl)-3,4-dimethyl­thio­phene-2,5-dicarboxamide
title_short N (2),N (2),N (5),N (5)-Tetra­kis(2-chloro­ethyl)-3,4-dimethyl­thio­phene-2,5-dicarboxamide
title_sort n (2),n (2),n (5),n (5)-tetra­kis(2-chloro­ethyl)-3,4-dimethyl­thio­phene-2,5-dicarboxamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980083/
https://www.ncbi.nlm.nih.gov/pubmed/21579991
http://dx.doi.org/10.1107/S1600536809052374
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AT zhouchenghe n2n2n5n5tetrakis2chloroethyl34dimethylthiophene25dicarboxamide

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