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Home  > Chemistry  > Heterocyclic Building Blocks  > Piperidines  > 4-Amino-1-(1-Boc-piperidin-4-yl)-1H-pyrazole

AB44804

1029413-55-5 | 4-Amino-1-(1-Boc-piperidin-4-yl)-1H-pyrazole

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $25.00 $18.00 -   +
1g 95% in stock $32.00 $23.00 -   +
5g 95% in stock $103.00 $73.00 -   +
10g 95% in stock $205.00 $144.00 -   +
100g 95% in stock $2,004.00 $1,403.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB44804
Chemical Name: 4-Amino-1-(1-Boc-piperidin-4-yl)-1H-pyrazole
CAS Number: 1029413-55-5
Molecular Formula: C13H22N4O2
Molecular Weight: 266.3394
MDL Number: MFCD10687120
SMILES: Nc1cnn(c1)C1CCN(CC1)C(=O)OC(C)(C)C

 

Computed Properties
Complexity: 321  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 19  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 3  
XLogP3: 0.9  

 

 

Upstream Synthesis Route
  • The tert-butyl 4-(4-amino-1H-pyrazol-1-yl)piperidine-1-carboxylate is a versatile compound that finds widespread application in chemical synthesis. This compound serves as a valuable building block for the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it an essential component in the development of novel molecules with potentially beneficial properties.In chemical synthesis, tert-butyl 4-(4-amino-1H-pyrazol-1-yl)piperidine-1-carboxylate can be utilized as a key intermediate in the preparation of bioactive molecules, such as inhibitors, catalysts, and ligands. Its functional groups enable the modification of its structure through various chemical reactions, allowing for the introduction of specific features or properties into the final product. By incorporating this compound into synthetic pathways, chemists can access a diverse array of derivatives and analogs that may exhibit enhanced efficacy or selectivity in their intended applications.Moreover, the tert-butyl 4-(4-amino-1H-pyrazol-1-yl)piperidine-1-carboxylate can participate in multistep synthesis strategies to construct complex molecular scaffolds efficiently. Its stable tert-butyl protecting group ensures the preservation of its core functionality during subsequent transformations, contributing to the overall synthetic efficiency and yield of the desired products. Through strategic manipulation of its molecular structure, chemists can harness the synthetic potential of this compound to access new chemical entities with improved biological activities or physicochemical properties.Overall, the tert-butyl 4-(4-amino-1H-pyrazol-1-yl)piperidine-1-carboxylate represents a valuable tool in the arsenal of synthetic chemists for the assembly of diverse chemical structures with tailored functionalities and applications. Its versatility and reactivity make it a valuable asset in the pursuit of innovative solutions in pharmaceutical, agricultural, and materials science research.
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