Thioureas
Thioureas are a class of organic compounds characterized by the presence of a sulfur atom bonded to both nitrogen and carbon atoms, forming a -NSR group. These molecules exhibit a wide range of applications due to their unique structural features and chemical properties. Commonly used in pharmaceuticals as antimicrobial agents, thioureas also find applications in agricultural pesticides, fungicides, and herbicides.
In the field of catalysis, thioureas serve as efficient bifunctional catalysts for various reactions, including the synthesis of amino acids and peptides. They are also employed in the production of polyurethane foams due to their ability to promote rapid urethane formation under mild conditions. Additionally, certain thiourea derivatives can act as antioxidants, protecting materials from oxidative degradation.
The diverse chemical reactivity of thioureas is attributed to their ability to interact with a wide array of metal ions, making them valuable in the design and synthesis of complex molecules. Their unique properties make thioureas indispensable in both academic research and industrial processes across multiple sectors.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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cyclobutylthiourea | 572889-33-9 | C5H10N2S |
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[3-(dimethylamino)propyl]thiourea | 196809-80-0 | C6H15N3S |
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(2-Diisopropylamino-ethyl)thiourea | 886363-52-6 | C9H21N3S |
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1-(adamantan-1-yl)-3-methylthiourea | 25444-83-1 | C12H20N2S |
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Isophorene | 57898-05-2 | C14H28N4S2 |
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59814-60-7 | C7H12N2S |
Related Literature
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James D. Kirkham,Patrick M. Delaney,George J. Ellames,Eleanor C. Row,Joseph P. A. Harrity Chem. Commun., 2010,46, 5154-5156
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S. Amaresh,K. Karthikeyan,K. J. Kim,Y. S. Lee RSC Adv., 2014,4, 23107-23115
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Muniyandi Sankaralingam,So Hyun Jeon,Yong-Min Lee,Mi Sook Seo,Wonwoo Nam Dalton Trans., 2016,45, 376-383
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