Thioureas
Thioureas are a class of organic compounds characterized by the presence of a sulfur atom bonded to an amino group and another carbon or heteroatom, forming a thiourea functional group (R-S-NHR'). These compounds have diverse applications in various fields including pharmaceuticals, agrochemicals, dyes, and industrial catalysts. In the pharmaceutical industry, thioureas are often used as intermediates for drug synthesis due to their unique reactivity. They can act as chelating agents, providing coordination chemistry capabilities that facilitate interactions with metal ions. Additionally, thioureas exhibit potential anti-inflammatory, antiviral, and anticancer activities, making them valuable in the development of new therapeutic agents. Their structural flexibility allows for modification into a wide range of derivatives, enhancing their applicability across different areas of research and industrial processes.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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1-(adamantan-1-yl)-3-(prop-2-en-1-yl)thiourea | 29456-83-5 | C14H22N2S |
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(Pentan-3-yl)thiourea | 854654-68-5 | C6H14N2S |
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Thiourea, [2-(dimethylamino)ethyl]- | 86114-63-8 | C5H13N3S |
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(2-cyclopropylethyl)thiourea | 1467394-84-8 | C6H12N2S |
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(2-methylcyclopropyl)thiourea | 1248026-56-3 | C5H10N2S |
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3-cyano-1-methylthiourea | 78286-57-4 | C3H5N3S |
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Thiourea, (2-aminoethyl)- | 3685-60-7 | C3H9N3S |
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Thiourea, [3-(methylthio)propyl]- | 37791-18-7 | C5H12N2S2 |
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thiourea, N,N'-dicyclohexyl- | 1212-29-9 | C13H24N2S |
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1-Isopropylthiourea | 1719-76-2 | C4H10N2S |
Related Literature
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José M. Rivera,Mariana Martín-Hidalgo,Jean C. Rivera-Ríos Org. Biomol. Chem., 2012,10, 7562-7565
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Fuming Xiao,Mengzhu Wang,Yunxiang Lei,Wenbo Dai,Yunbing Zhou,Miaochang Liu,Wenxia Gao,Xiaobo Huang,Huayue Wu J. Mater. Chem. C, 2020,8, 17410-17416
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