(Z)-Benzyl 2-(5-methyl-2-oxoindolin-3-ylidene)-hydrazinecarbodithioate
The title compound, C17H15N3OS2 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 intramolecula...
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International Union of Crystallography
2023
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Online Access: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85173249817&doi=10.1107%2fS2414314623007824&partnerID=40&md5=294e3ea4de902b72d6666ae00898858c |
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2-s2.0-85173249817 Abdul Manan M.A.F.; Cordes D.B.; McKay A.P.; Mohammat M.F.; Mohd Aluwi M.F.F.; Jumali N.S. (Z)-Benzyl 2-(5-methyl-2-oxoindolin-3-ylidene)-hydrazinecarbodithioate 2023 IUCrData 8 9 10.1107/S2414314623007824 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85173249817&doi=10.1107%2fS2414314623007824&partnerID=40&md5=294e3ea4de902b72d6666ae00898858c The title compound, C17H15N3OS2 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. © 2023 The Author(s). International Union of Crystallography 24143146 English Data paper All Open Access; Gold Open Access; Green Open Access |
author |
Abdul Manan M.A.F.; Cordes D.B.; McKay A.P.; Mohammat M.F.; Mohd Aluwi M.F.F.; Jumali N.S. |
spellingShingle |
Abdul Manan M.A.F.; Cordes D.B.; McKay A.P.; Mohammat M.F.; Mohd Aluwi M.F.F.; Jumali N.S. (Z)-Benzyl 2-(5-methyl-2-oxoindolin-3-ylidene)-hydrazinecarbodithioate |
author_facet |
Abdul Manan M.A.F.; Cordes D.B.; McKay A.P.; Mohammat M.F.; Mohd Aluwi M.F.F.; Jumali N.S. |
author_sort |
Abdul Manan M.A.F.; Cordes D.B.; McKay A.P.; Mohammat M.F.; Mohd Aluwi M.F.F.; Jumali N.S. |
title |
(Z)-Benzyl 2-(5-methyl-2-oxoindolin-3-ylidene)-hydrazinecarbodithioate |
title_short |
(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_sort |
(Z)-Benzyl 2-(5-methyl-2-oxoindolin-3-ylidene)-hydrazinecarbodithioate |
publishDate |
2023 |
container_title |
IUCrData |
container_volume |
8 |
container_issue |
9 |
doi_str_mv |
10.1107/S2414314623007824 |
url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85173249817&doi=10.1107%2fS2414314623007824&partnerID=40&md5=294e3ea4de902b72d6666ae00898858c |
description |
The title compound, C17H15N3OS2 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. © 2023 The Author(s). |
publisher |
International Union of Crystallography |
issn |
24143146 |
language |
English |
format |
Data paper |
accesstype |
All Open Access; Gold Open Access; Green Open Access |
record_format |
scopus |
collection |
Scopus |
_version_ |
1809677588285620224 |