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AV57193

1152940-07-2 | 1-(pyridin-3-ylmethyl)-1H-pyrazol-4-amine

Packsize Purity Availability Price Discounted Price    Quantity
50mg 95% 1 week $183.00 $128.00 -   +
100mg 95% 1 week $249.00 $174.00 -   +
250mg 95% 1 week $333.00 $233.00 -   +
500mg 95% 1 week $581.00 $407.00 -   +
1g 95% 1 week $757.00 $530.00 -   +
2.5g 95% 1 week $1,438.00 $1,007.00 -   +
5g 95% 1 week $2,102.00 $1,471.00 -   +
10g 95% 1 week $3,094.00 $2,166.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AV57193
Chemical Name: 1-(pyridin-3-ylmethyl)-1H-pyrazol-4-amine
CAS Number: 1152940-07-2
Molecular Formula: C9H10N4
Molecular Weight: 174.2025
MDL Number: MFCD11128207
SMILES: Nc1cnn(c1)Cc1cccnc1

 

Computed Properties
Complexity: 162  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 0.1  

 

 

Upstream Synthesis Route
  • The compound 1-(Pyridin-3-ylmethyl)-1H-pyrazol-4-amine, often referred to as $name$, serves as a versatile building block in chemical synthesis. Its unique structure containing both a pyridine and a pyrazole ring provides a platform for the creation of diverse chemical structures with potential applications in pharmaceuticals, agrochemicals, and materials science.In chemical synthesis, $name$ can be utilized as a key intermediate for the preparation of various biologically active compounds. Its amino group enables the introduction of additional functional groups through derivatization, facilitating the synthesis of new drug candidates or molecular probes for biological studies. The presence of the pyrazole moiety also contributes to the compound's reactivity, allowing for the formation of complex molecular frameworks through cyclization or cross-coupling reactions.Furthermore, the conjugation of the pyridine and pyrazole rings in $name$ offers opportunities for the development of ligands for coordination chemistry or catalysts for organic transformations. By judiciously modifying the substituents on the aromatic rings, chemists can fine-tune the properties of the resulting molecules for specific applications, such as asymmetric catalysis or materials design.Overall, 1-(Pyridin-3-ylmethyl)-1H-pyrazol-4-amine is a valuable tool in the hands of synthetic chemists, enabling the construction of complex molecular architectures and the exploration of new chemical space for various scientific and technological endeavors.
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