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AB47152

79-19-6 | Thiosemicarbazide

Packsize Purity Availability Price Discounted Price    Quantity
25g 98% in stock $20.00 $14.00 -   +

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Description
Catalog Number: AB47152
Chemical Name: Thiosemicarbazide
CAS Number: 79-19-6
Molecular Formula: CH5N3S
Molecular Weight: 91.1355
MDL Number: MFCD00007620
SMILES: NNC(=S)N

 

Computed Properties
Complexity: 42.2  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 5  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 3  
XLogP3: -1.2  

 

 

Upstream Synthesis Route
  • Thiosemicarbazide is a versatile compound that finds wide applications in chemical synthesis. It is commonly used as a building block in the preparation of various heterocyclic compounds, including thiazoles, thiadiazoles, and thiazolidinones. The versatility of thiosemicarbazide lies in its unique structure, which contains both an amino group and a thioamide functional group. These functional groups can undergo a variety of chemical transformations, making thiosemicarbazide a valuable starting material for the synthesis of diverse organic molecules.One of the key applications of thiosemicarbazide in chemical synthesis is its use in the preparation of biologically active compounds. Thiosemicarbazide derivatives have demonstrated a wide range of pharmacological activities, including antimicrobial, antiviral, anticancer, and anticonvulsant properties. By modifying the structure of thiosemicarbazide and introducing various substituents, chemists can tailor the properties of the resulting compounds to target specific biological activities.In addition to its pharmacological applications, thiosemicarbazide is also employed in the synthesis of materials with industrial significance. For example, thiosemicarbazide derivatives have been utilized in the preparation of corrosion inhibitors, fluorescent dyes, and metal complexes. The ability of thiosemicarbazide to chelate metal ions makes it a valuable ligand in coordination chemistry, allowing for the formation of stable complexes with various metal ions.Overall, the diverse applications of thiosemicarbazide in chemical synthesis highlight its importance as a versatile building block in the preparation of biologically active compounds and functional materials. Its unique structural features and reactivity make it a valuable tool for the synthesis of a wide range of organic molecules with tailored properties and applications.
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