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(E)-5-(3,5-Dimethylphenyl)-N-[4-(methylsulfanyl)benzylidene]-1,3,4-thiadiazol-2-amine
The title compound, C(18)H(17)N(3)S(2), was synthesized by the reaction of 5-(3,5-dimethylphenyl)-1,3,4-thiadiazol-2-amine and 4-(methylsulfanyl)benzaldehyde. An intramolecular C—H⋯S hydrogen bond results in the formation of a planar (r.m.s. deviation = 0.003 Å) five-membered ring. In the crys...
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/PMC2979762/ https://www.ncbi.nlm.nih.gov/pubmed/21579829 http://dx.doi.org/10.1107/S1600536810001558 |
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author | Hu, Jun Ji, Jin-xiu Zhou, Ying Wang, Ji-kui Xu, Yan-hua |
author_facet | Hu, Jun Ji, Jin-xiu Zhou, Ying Wang, Ji-kui Xu, Yan-hua |
author_sort | Hu, Jun |
collection | PubMed |
description | The title compound, C(18)H(17)N(3)S(2), was synthesized by the reaction of 5-(3,5-dimethylphenyl)-1,3,4-thiadiazol-2-amine and 4-(methylsulfanyl)benzaldehyde. An intramolecular C—H⋯S hydrogen bond results in the formation of a planar (r.m.s. deviation = 0.003 Å) five-membered ring. In the crystal structure, intermolecular C—H⋯N hydrogen bonds link the molecules to form layers parallel to (011). |
format | Text |
id | pubmed-2979762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29797622010-12-30 (E)-5-(3,5-Dimethylphenyl)-N-[4-(methylsulfanyl)benzylidene]-1,3,4-thiadiazol-2-amine Hu, Jun Ji, Jin-xiu Zhou, Ying Wang, Ji-kui Xu, Yan-hua Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(18)H(17)N(3)S(2), was synthesized by the reaction of 5-(3,5-dimethylphenyl)-1,3,4-thiadiazol-2-amine and 4-(methylsulfanyl)benzaldehyde. An intramolecular C—H⋯S hydrogen bond results in the formation of a planar (r.m.s. deviation = 0.003 Å) five-membered ring. In the crystal structure, intermolecular C—H⋯N hydrogen bonds link the molecules to form layers parallel to (011). International Union of Crystallography 2010-01-20 /pmc/articles/PMC2979762/ /pubmed/21579829 http://dx.doi.org/10.1107/S1600536810001558 Text en © Hu 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 Hu, Jun Ji, Jin-xiu Zhou, Ying Wang, Ji-kui Xu, Yan-hua (E)-5-(3,5-Dimethylphenyl)-N-[4-(methylsulfanyl)benzylidene]-1,3,4-thiadiazol-2-amine |
title | (E)-5-(3,5-Dimethylphenyl)-N-[4-(methylsulfanyl)benzylidene]-1,3,4-thiadiazol-2-amine |
title_full | (E)-5-(3,5-Dimethylphenyl)-N-[4-(methylsulfanyl)benzylidene]-1,3,4-thiadiazol-2-amine |
title_fullStr | (E)-5-(3,5-Dimethylphenyl)-N-[4-(methylsulfanyl)benzylidene]-1,3,4-thiadiazol-2-amine |
title_full_unstemmed | (E)-5-(3,5-Dimethylphenyl)-N-[4-(methylsulfanyl)benzylidene]-1,3,4-thiadiazol-2-amine |
title_short | (E)-5-(3,5-Dimethylphenyl)-N-[4-(methylsulfanyl)benzylidene]-1,3,4-thiadiazol-2-amine |
title_sort | (e)-5-(3,5-dimethylphenyl)-n-[4-(methylsulfanyl)benzylidene]-1,3,4-thiadiazol-2-amine |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979762/ https://www.ncbi.nlm.nih.gov/pubmed/21579829 http://dx.doi.org/10.1107/S1600536810001558 |
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