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[(Methylcarbamothioyl)disulfanyl]methyl N-methylcarbamodithioate
The title compound, C(5)H(10)N(2)S(5), was unintentionally obtained as the product of an attempted synthesis of a methylcarbamodithioic acid using methylamine and carbon disulfide. In the molecule, two dithiocarbamate groups are bridged by a –CH(2)S– unit. The C—S—S—C torsion angle is −90.13 (11...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983331/ https://www.ncbi.nlm.nih.gov/pubmed/21587641 http://dx.doi.org/10.1107/S160053681003833X |
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author | Khan, Hizbullah Aziz, Muhammad Neuhausen, Christine Murtaza, Ghulam Shaheen, Farkhanda |
author_facet | Khan, Hizbullah Aziz, Muhammad Neuhausen, Christine Murtaza, Ghulam Shaheen, Farkhanda |
author_sort | Khan, Hizbullah |
collection | PubMed |
description | The title compound, C(5)H(10)N(2)S(5), was unintentionally obtained as the product of an attempted synthesis of a methylcarbamodithioic acid using methylamine and carbon disulfide. In the molecule, two dithiocarbamate groups are bridged by a –CH(2)S– unit. The C—S—S—C torsion angle is −90.13 (11)°. The crystal structure is stabilized by N—H⋯S interactions between neighbouring molecules. An intramolecular N—H⋯S hydrogen bond also occurs. |
format | Text |
id | pubmed-2983331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29833312010-12-30 [(Methylcarbamothioyl)disulfanyl]methyl N-methylcarbamodithioate Khan, Hizbullah Aziz, Muhammad Neuhausen, Christine Murtaza, Ghulam Shaheen, Farkhanda Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(5)H(10)N(2)S(5), was unintentionally obtained as the product of an attempted synthesis of a methylcarbamodithioic acid using methylamine and carbon disulfide. In the molecule, two dithiocarbamate groups are bridged by a –CH(2)S– unit. The C—S—S—C torsion angle is −90.13 (11)°. The crystal structure is stabilized by N—H⋯S interactions between neighbouring molecules. An intramolecular N—H⋯S hydrogen bond also occurs. International Union of Crystallography 2010-09-30 /pmc/articles/PMC2983331/ /pubmed/21587641 http://dx.doi.org/10.1107/S160053681003833X Text en © Khan 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 Khan, Hizbullah Aziz, Muhammad Neuhausen, Christine Murtaza, Ghulam Shaheen, Farkhanda [(Methylcarbamothioyl)disulfanyl]methyl N-methylcarbamodithioate |
title | [(Methylcarbamothioyl)disulfanyl]methyl N-methylcarbamodithioate |
title_full | [(Methylcarbamothioyl)disulfanyl]methyl N-methylcarbamodithioate |
title_fullStr | [(Methylcarbamothioyl)disulfanyl]methyl N-methylcarbamodithioate |
title_full_unstemmed | [(Methylcarbamothioyl)disulfanyl]methyl N-methylcarbamodithioate |
title_short | [(Methylcarbamothioyl)disulfanyl]methyl N-methylcarbamodithioate |
title_sort | [(methylcarbamothioyl)disulfanyl]methyl n-methylcarbamodithioate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983331/ https://www.ncbi.nlm.nih.gov/pubmed/21587641 http://dx.doi.org/10.1107/S160053681003833X |
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