(2E)-2-(5-Bromo-2-hydroxy-3-methoxybenzylidene)-N-cyclohexylhydrazinecarbothioamide

The title compound, C15H20BrN3O2S, crystallizes in the thioamide form and adopts an E,E conformation with respect to the azomethine and hydrazinic bonds, respectively. The molecules are paired through N—H...O and O—H...S hydrogen bonds, leading to the formation of centros...

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Main Authors: Jinsa Mary Jacob, M. R. Prathapachandra Kurup
Format: Article
Language:English
Published: International Union of Crystallography 2012-03-01
Series:Acta Crystallographica Section E
Online Access:http://scripts.iucr.org/cgi-bin/paper?S1600536812007039
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author Jinsa Mary Jacob
M. R. Prathapachandra Kurup
author_facet Jinsa Mary Jacob
M. R. Prathapachandra Kurup
author_sort Jinsa Mary Jacob
collection DOAJ
description The title compound, C15H20BrN3O2S, crystallizes in the thioamide form and adopts an E,E conformation with respect to the azomethine and hydrazinic bonds, respectively. The molecules are paired through N—H...O and O—H...S hydrogen bonds, leading to the formation of centrosymmetric dimers in the crystal. These dimers are stacked along the a axis and are interconnected through N—H...S hydrogen bonds to generate polymeric chains. The structure also features C—H...π interactions. An intramolecular O—H...O bond is also present.
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spelling doaj.art-daf053c5bac943fe822b283b878d91e42022-12-22T04:10:27ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682012-03-01683o836o83710.1107/S1600536812007039(2E)-2-(5-Bromo-2-hydroxy-3-methoxybenzylidene)-N-cyclohexylhydrazinecarbothioamideJinsa Mary JacobM. R. Prathapachandra KurupThe title compound, C15H20BrN3O2S, crystallizes in the thioamide form and adopts an E,E conformation with respect to the azomethine and hydrazinic bonds, respectively. The molecules are paired through N—H...O and O—H...S hydrogen bonds, leading to the formation of centrosymmetric dimers in the crystal. These dimers are stacked along the a axis and are interconnected through N—H...S hydrogen bonds to generate polymeric chains. The structure also features C—H...π interactions. An intramolecular O—H...O bond is also present.http://scripts.iucr.org/cgi-bin/paper?S1600536812007039
spellingShingle Jinsa Mary Jacob
M. R. Prathapachandra Kurup
(2E)-2-(5-Bromo-2-hydroxy-3-methoxybenzylidene)-N-cyclohexylhydrazinecarbothioamide
Acta Crystallographica Section E
title (2E)-2-(5-Bromo-2-hydroxy-3-methoxybenzylidene)-N-cyclohexylhydrazinecarbothioamide
title_full (2E)-2-(5-Bromo-2-hydroxy-3-methoxybenzylidene)-N-cyclohexylhydrazinecarbothioamide
title_fullStr (2E)-2-(5-Bromo-2-hydroxy-3-methoxybenzylidene)-N-cyclohexylhydrazinecarbothioamide
title_full_unstemmed (2E)-2-(5-Bromo-2-hydroxy-3-methoxybenzylidene)-N-cyclohexylhydrazinecarbothioamide
title_short (2E)-2-(5-Bromo-2-hydroxy-3-methoxybenzylidene)-N-cyclohexylhydrazinecarbothioamide
title_sort 2e 2 5 bromo 2 hydroxy 3 methoxybenzylidene n cyclohexylhydrazinecarbothioamide
url http://scripts.iucr.org/cgi-bin/paper?S1600536812007039
work_keys_str_mv AT jinsamaryjacob 2e25bromo2hydroxy3methoxybenzylidenencyclohexylhydrazinecarbothioamide
AT mrprathapachandrakurup 2e25bromo2hydroxy3methoxybenzylidenencyclohexylhydrazinecarbothioamide