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Diethyl 3,4-bis(acetoxy­meth­yl)thieno[2,3-b]thio­phene-2,5-dicarboxyl­ate

In the title compound, C(18)H(20)O(8)S(2), the dihedral angle between the two thio­phene rings is 2.33 (7)°. The methyl C atoms of the ester groups are disordered over two positions; the site-occupancy factors of the terminal methyl C atoms are 0.632 (18):0.368 (18) and 0.623 (17):0.377 (17). The mo...

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Autores principales: Gunasekaran, B., Sureshbabu, R., Mohanakrishnan, A. K., Chakkaravarthi, G., Manivannan, V.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970297/
https://www.ncbi.nlm.nih.gov/pubmed/21577910
http://dx.doi.org/10.1107/S1600536809036149
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author Gunasekaran, B.
Sureshbabu, R.
Mohanakrishnan, A. K.
Chakkaravarthi, G.
Manivannan, V.
author_facet Gunasekaran, B.
Sureshbabu, R.
Mohanakrishnan, A. K.
Chakkaravarthi, G.
Manivannan, V.
author_sort Gunasekaran, B.
collection PubMed
description In the title compound, C(18)H(20)O(8)S(2), the dihedral angle between the two thio­phene rings is 2.33 (7)°. The methyl C atoms of the ester groups are disordered over two positions; the site-occupancy factors of the terminal methyl C atoms are 0.632 (18):0.368 (18) and 0.623 (17):0.377 (17). The mol­ecular structure is stabilized by weak intra­molecular C—H⋯O inter­actions and the crystal structure is stabilized through weak inter­molecular C—H⋯O inter­actions.
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spelling pubmed-29702972010-12-30 Diethyl 3,4-bis(acetoxy­meth­yl)thieno[2,3-b]thio­phene-2,5-dicarboxyl­ate Gunasekaran, B. Sureshbabu, R. Mohanakrishnan, A. K. Chakkaravarthi, G. Manivannan, V. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(18)H(20)O(8)S(2), the dihedral angle between the two thio­phene rings is 2.33 (7)°. The methyl C atoms of the ester groups are disordered over two positions; the site-occupancy factors of the terminal methyl C atoms are 0.632 (18):0.368 (18) and 0.623 (17):0.377 (17). The mol­ecular structure is stabilized by weak intra­molecular C—H⋯O inter­actions and the crystal structure is stabilized through weak inter­molecular C—H⋯O inter­actions. International Union of Crystallography 2009-09-12 /pmc/articles/PMC2970297/ /pubmed/21577910 http://dx.doi.org/10.1107/S1600536809036149 Text en © Gunasekaran 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
Gunasekaran, B.
Sureshbabu, R.
Mohanakrishnan, A. K.
Chakkaravarthi, G.
Manivannan, V.
Diethyl 3,4-bis(acetoxy­meth­yl)thieno[2,3-b]thio­phene-2,5-dicarboxyl­ate
title Diethyl 3,4-bis(acetoxy­meth­yl)thieno[2,3-b]thio­phene-2,5-dicarboxyl­ate
title_full Diethyl 3,4-bis(acetoxy­meth­yl)thieno[2,3-b]thio­phene-2,5-dicarboxyl­ate
title_fullStr Diethyl 3,4-bis(acetoxy­meth­yl)thieno[2,3-b]thio­phene-2,5-dicarboxyl­ate
title_full_unstemmed Diethyl 3,4-bis(acetoxy­meth­yl)thieno[2,3-b]thio­phene-2,5-dicarboxyl­ate
title_short Diethyl 3,4-bis(acetoxy­meth­yl)thieno[2,3-b]thio­phene-2,5-dicarboxyl­ate
title_sort diethyl 3,4-bis(acetoxy­meth­yl)thieno[2,3-b]thio­phene-2,5-dicarboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970297/
https://www.ncbi.nlm.nih.gov/pubmed/21577910
http://dx.doi.org/10.1107/S1600536809036149
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