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(Z)-Benzyl 2-(5-methyl-2-oxoindolin-3-ylidene)hydrazinecarbodithioate
The title compound, C(17)H(15)N(3)OS(2) was obtained from the condensation reaction of S-benzyldithiocarbazate and 5-methylisatin. In the solid-state, the molecule adopts a Z configuration with the 5-methylisatin and dithiocarbazate groups located on the same side of the C=N bond, involving a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10561232/ https://www.ncbi.nlm.nih.gov/pubmed/37818467 http://dx.doi.org/10.1107/S2414314623007824 |
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author | Abdul Manan, Mohd Abdul Fatah Cordes, David B. McKay, Aidan P. Mohammat, Mohd Fazli Mohd Aluwi, Mohd Fadhlizil Fasihi Jumali, Nor Saliyana |
author_facet | Abdul Manan, Mohd Abdul Fatah Cordes, David B. McKay, Aidan P. Mohammat, Mohd Fazli Mohd Aluwi, Mohd Fadhlizil Fasihi Jumali, Nor Saliyana |
author_sort | Abdul Manan, Mohd Abdul Fatah |
collection | PubMed |
description | The title compound, C(17)H(15)N(3)OS(2) was obtained from the condensation reaction of S-benzyldithiocarbazate and 5-methylisatin. In the solid-state, the molecule adopts a Z configuration with the 5-methylisatin and dithiocarbazate groups located on the same side of the C=N bond, involving an intramolecular N—H⋯O hydrogen bond. [Image: see text] |
format | Online Article Text |
id | pubmed-10561232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-105612322023-10-10 (Z)-Benzyl 2-(5-methyl-2-oxoindolin-3-ylidene)hydrazinecarbodithioate Abdul Manan, Mohd Abdul Fatah Cordes, David B. McKay, Aidan P. Mohammat, Mohd Fazli Mohd Aluwi, Mohd Fadhlizil Fasihi Jumali, Nor Saliyana IUCrdata Data Reports The title compound, C(17)H(15)N(3)OS(2) was obtained from the condensation reaction of S-benzyldithiocarbazate and 5-methylisatin. In the solid-state, the molecule adopts a Z configuration with the 5-methylisatin and dithiocarbazate groups located on the same side of the C=N bond, involving an intramolecular N—H⋯O hydrogen bond. [Image: see text] International Union of Crystallography 2023-09-12 /pmc/articles/PMC10561232/ /pubmed/37818467 http://dx.doi.org/10.1107/S2414314623007824 Text en © Abdul Manan et al. 2023 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Data Reports Abdul Manan, Mohd Abdul Fatah Cordes, David B. McKay, Aidan P. Mohammat, Mohd Fazli Mohd Aluwi, Mohd Fadhlizil Fasihi Jumali, Nor Saliyana (Z)-Benzyl 2-(5-methyl-2-oxoindolin-3-ylidene)hydrazinecarbodithioate |
title | (Z)-Benzyl 2-(5-methyl-2-oxoindolin-3-ylidene)hydrazinecarbodithioate |
title_full | (Z)-Benzyl 2-(5-methyl-2-oxoindolin-3-ylidene)hydrazinecarbodithioate |
title_fullStr | (Z)-Benzyl 2-(5-methyl-2-oxoindolin-3-ylidene)hydrazinecarbodithioate |
title_full_unstemmed | (Z)-Benzyl 2-(5-methyl-2-oxoindolin-3-ylidene)hydrazinecarbodithioate |
title_short | (Z)-Benzyl 2-(5-methyl-2-oxoindolin-3-ylidene)hydrazinecarbodithioate |
title_sort | (z)-benzyl 2-(5-methyl-2-oxoindolin-3-ylidene)hydrazinecarbodithioate |
topic | Data Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10561232/ https://www.ncbi.nlm.nih.gov/pubmed/37818467 http://dx.doi.org/10.1107/S2414314623007824 |
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