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Home  > 5-Pyridin-4-yl-2H-pyrazol-3-ylamine

AB50835

91912-53-7 | 5-Pyridin-4-yl-2H-pyrazol-3-ylamine

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $15.00 $11.00 -   +
1g 98% in stock $34.00 $24.00 -   +
5g 98% in stock $157.00 $110.00 -   +
10g 98% in stock $314.00 $220.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB50835
Chemical Name: 5-Pyridin-4-yl-2H-pyrazol-3-ylamine
CAS Number: 91912-53-7
Molecular Formula: C8H8N4
Molecular Weight: 160.1759
MDL Number: MFCD06738752
SMILES: Nc1[nH]nc(c1)c1ccncc1

 

Computed Properties
Complexity: 144  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 1  
XLogP3: 0.5  

 

 

Upstream Synthesis Route
  • The compound 3-(Pyridin-4-yl)-1H-pyrazol-5-amine plays a crucial role in chemical synthesis as a versatile building block. With its unique structure combining both pyridine and pyrazole moieties, this compound offers a wide range of possibilities for creating novel molecules in organic chemistry. One main application of 3-(Pyridin-4-yl)-1H-pyrazol-5-amine is its use as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its functional groups allow for facile modification through different chemical reactions, enabling the incorporation of specific properties or activities desired in the final products.Furthermore, this compound can serve as a ligand in coordination chemistry, forming complexes with transition metals for applications in catalysis or material science. Its ability to chelate metal ions opens up avenues for designing new catalysts or functional materials with tailored properties.In addition, 3-(Pyridin-4-yl)-1H-pyrazol-5-amine can also be employed in the synthesis of fluorescent dyes or probes for biological imaging studies. By attaching fluorophores or other reporter groups to this core structure, researchers can develop molecular probes for detecting specific targets in biological systems with high sensitivity and selectivity.
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