5-Bromo-1H-indole-3-carbaldehyde thio­semicarbazone

In the essentially planar title mol­ecule, C(10)H(9)BrN(4)S, the C=N double bond is in a trans configuration. In the crystal structure, the S atom acts as a hydrogen-bond acceptor for the aromatic NH, aliphatic NH and terminal NH(2) groups of three symmetry-related mol­ecules, forming a weak hydroge...

Descripción completa

Detalles Bibliográficos
Autores principales: Rizal, Mohd. Razali, Ali, Hapipah Mohd., Ng, Seik Weng
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961179/
https://www.ncbi.nlm.nih.gov/pubmed/21202400
http://dx.doi.org/10.1107/S160053680801101X
_version_ 1782188920609439744
author Rizal, Mohd. Razali
Ali, Hapipah Mohd.
Ng, Seik Weng
author_facet Rizal, Mohd. Razali
Ali, Hapipah Mohd.
Ng, Seik Weng
author_sort Rizal, Mohd. Razali
collection PubMed
description In the essentially planar title mol­ecule, C(10)H(9)BrN(4)S, the C=N double bond is in a trans configuration. In the crystal structure, the S atom acts as a hydrogen-bond acceptor for the aromatic NH, aliphatic NH and terminal NH(2) groups of three symmetry-related mol­ecules, forming a weak hydrogen-bonded layer structure.
format Text
id pubmed-2961179
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29611792010-12-30 5-Bromo-1H-indole-3-carbaldehyde thio­semicarbazone Rizal, Mohd. Razali Ali, Hapipah Mohd. Ng, Seik Weng Acta Crystallogr Sect E Struct Rep Online Organic Papers In the essentially planar title mol­ecule, C(10)H(9)BrN(4)S, the C=N double bond is in a trans configuration. In the crystal structure, the S atom acts as a hydrogen-bond acceptor for the aromatic NH, aliphatic NH and terminal NH(2) groups of three symmetry-related mol­ecules, forming a weak hydrogen-bonded layer structure. International Union of Crystallography 2008-04-26 /pmc/articles/PMC2961179/ /pubmed/21202400 http://dx.doi.org/10.1107/S160053680801101X Text en © Rizal et al. 2008 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
Rizal, Mohd. Razali
Ali, Hapipah Mohd.
Ng, Seik Weng
5-Bromo-1H-indole-3-carbaldehyde thio­semicarbazone
title 5-Bromo-1H-indole-3-carbaldehyde thio­semicarbazone
title_full 5-Bromo-1H-indole-3-carbaldehyde thio­semicarbazone
title_fullStr 5-Bromo-1H-indole-3-carbaldehyde thio­semicarbazone
title_full_unstemmed 5-Bromo-1H-indole-3-carbaldehyde thio­semicarbazone
title_short 5-Bromo-1H-indole-3-carbaldehyde thio­semicarbazone
title_sort 5-bromo-1h-indole-3-carbaldehyde thio­semicarbazone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961179/
https://www.ncbi.nlm.nih.gov/pubmed/21202400
http://dx.doi.org/10.1107/S160053680801101X
work_keys_str_mv AT rizalmohdrazali 5bromo1hindole3carbaldehydethiosemicarbazone
AT alihapipahmohd 5bromo1hindole3carbaldehydethiosemicarbazone
AT ngseikweng 5bromo1hindole3carbaldehydethiosemicarbazone

Ejemplares similares