Eth­oxy­carbonyl­methyl 3-(4-chloro­benzyl­idene)dithio­carbazate

Mol­ecules of the title compound, C(12)H(13)ClN(2)O(2)S(2), are linked into centrosymmetric dimers by pairs of inter­molecular N—H⋯S hydrogen bonds. In the crystal structure, there are π–π stacking inter­actions between symmetry-related benzene rings with a centroid–centroid distance of 3.7305 (13) ...

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Detalles Bibliográficos
Autores principales: Tabatabaee, Masoumeh, Sharif, Mahboubeh A., Khalili, Robabeh, Parvez, Masood
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983262/
https://www.ncbi.nlm.nih.gov/pubmed/21587535
http://dx.doi.org/10.1107/S160053681003549X
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author Tabatabaee, Masoumeh
Sharif, Mahboubeh A.
Khalili, Robabeh
Parvez, Masood
author_facet Tabatabaee, Masoumeh
Sharif, Mahboubeh A.
Khalili, Robabeh
Parvez, Masood
author_sort Tabatabaee, Masoumeh
collection PubMed
description Mol­ecules of the title compound, C(12)H(13)ClN(2)O(2)S(2), are linked into centrosymmetric dimers by pairs of inter­molecular N—H⋯S hydrogen bonds. In the crystal structure, there are π–π stacking inter­actions between symmetry-related benzene rings with a centroid–centroid distance of 3.7305 (13) Å, a perpendicular distance between the planes of 3.2851 (9) Å and a slippage of 1.768 Å. The structure is further stabilized by weak inter­molecular C—H⋯O hydrogen bonds.
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spelling pubmed-29832622010-12-30 Eth­oxy­carbonyl­methyl 3-(4-chloro­benzyl­idene)dithio­carbazate Tabatabaee, Masoumeh Sharif, Mahboubeh A. Khalili, Robabeh Parvez, Masood Acta Crystallogr Sect E Struct Rep Online Organic Papers Mol­ecules of the title compound, C(12)H(13)ClN(2)O(2)S(2), are linked into centrosymmetric dimers by pairs of inter­molecular N—H⋯S hydrogen bonds. In the crystal structure, there are π–π stacking inter­actions between symmetry-related benzene rings with a centroid–centroid distance of 3.7305 (13) Å, a perpendicular distance between the planes of 3.2851 (9) Å and a slippage of 1.768 Å. The structure is further stabilized by weak inter­molecular C—H⋯O hydrogen bonds. International Union of Crystallography 2010-09-11 /pmc/articles/PMC2983262/ /pubmed/21587535 http://dx.doi.org/10.1107/S160053681003549X Text en © Tabatabaee 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
Tabatabaee, Masoumeh
Sharif, Mahboubeh A.
Khalili, Robabeh
Parvez, Masood
Eth­oxy­carbonyl­methyl 3-(4-chloro­benzyl­idene)dithio­carbazate
title Eth­oxy­carbonyl­methyl 3-(4-chloro­benzyl­idene)dithio­carbazate
title_full Eth­oxy­carbonyl­methyl 3-(4-chloro­benzyl­idene)dithio­carbazate
title_fullStr Eth­oxy­carbonyl­methyl 3-(4-chloro­benzyl­idene)dithio­carbazate
title_full_unstemmed Eth­oxy­carbonyl­methyl 3-(4-chloro­benzyl­idene)dithio­carbazate
title_short Eth­oxy­carbonyl­methyl 3-(4-chloro­benzyl­idene)dithio­carbazate
title_sort eth­oxy­carbonyl­methyl 3-(4-chloro­benzyl­idene)dithio­carbazate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983262/
https://www.ncbi.nlm.nih.gov/pubmed/21587535
http://dx.doi.org/10.1107/S160053681003549X
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AT parvezmasood ethoxycarbonylmethyl34chlorobenzylidenedithiocarbazate

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