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Home  > 4-Amino-3-Hydrazino-5-Mercapto-1,2,4-Triazole

AB66607

1750-12-5 | 4-Amino-3-Hydrazino-5-Mercapto-1,2,4-Triazole

Packsize Purity Availability Price Discounted Price    Quantity
1g 95% in stock $47.00 $33.00 -   +
5g 95% in stock $58.00 $40.00 -   +
25g 95% in stock $225.00 $157.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB66607
Chemical Name: 4-Amino-3-Hydrazino-5-Mercapto-1,2,4-Triazole
CAS Number: 1750-12-5
Molecular Formula: C2H6N6S
Molecular Weight: 146.17424
MDL Number: MFCD00003098
SMILES: Nn1c(=NN)[nH][nH]c1=S

 

Computed Properties
Complexity: 162  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 4  
Rotatable Bond Count: 1  
XLogP3: -1.1  

 

 

Upstream Synthesis Route
  • 4-Amino-3-Hydrazino-5-Mercapto-1,2,4-Triazole, commonly known as $name$, is a versatile chemical compound that finds extensive application in chemical synthesis processes. This compound serves as a crucial building block in the creation of various substances due to its unique molecular structure and reactivity.In chemical synthesis, $name$ is often used as a reagent or intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its hydrazino and mercapto functional groups make it a valuable precursor for the synthesis of heterocyclic compounds, which are essential in drug discovery and development.Moreover, the presence of amino and hydrazino moieties in $name$ enables it to participate in a wide range of organic reactions, including nucleophilic substitutions, condensations, and cyclizations. These reactions allow chemists to efficiently generate complex molecules with specific properties and functionalities.Overall, the application of 4-Amino-3-Hydrazino-5-Mercapto-1,2,4-Triazole in chemical synthesis plays a pivotal role in advancing research and innovation across various industries, making it a crucial component in molecular design and synthesis strategies.
Literature
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