Thiosemicarbazide
Chemical compound
From Wikipedia, the free encyclopedia
Thiosemicarbazide is the chemical compound with the formula H2NC(S)NHNH2. A white, odorless solid, it is related to thiourea (H2NC(S)NH2) by the insertion of an NH center. They are commonly used as ligands for transition metals.[2] Many thiosemicarbazides are known. These feature an organic substituent in place of one or more H's of the parent molecule. 4-Methyl-3-thiosemicarbazide is a simple example.
| Names | |
|---|---|
| Preferred IUPAC name
Hydrazinecarbothioamide[1] | |
| Other names
N-Aminothiourea, Aminothiourea | |
| Identifiers | |
3D model (JSmol) |
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| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.001.077 |
| EC Number |
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PubChem CID |
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| UNII | |
| UN number | 2811 2771 |
CompTox Dashboard (EPA) |
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| Properties | |
| CH5N3S | |
| Molar mass | 91.13 g·mol−1 |
| Appearance | white solid |
| Density | 1.465 g/cm3 |
| Melting point | 183 °C (361 °F; 456 K) |
| Hazards | |
| GHS labelling: | |
| Danger | |
| H300, H412 | |
| P264, P270, P273, P301+P310, P321, P330, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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According to X-ray crystallography, the CSN3 core of the molecule is almost planar as are the three H atoms nearest the thiocarbonyl group.[3] This can be explained by models of electron delocalisation.
Reactions
Thiosemicarbazides are precursors to thiosemicarbazones. They are precursors to heterocycles.[4] Formylation of thiosemicarbazide provides access to triazole.[5]
