logo
Home  > Chemistry  > Heterocyclic Building Blocks  > Pyridines  > 5-Amino-2-(4-BOC-piperazino)pyridine

AA23804

119285-07-3 | 5-Amino-2-(4-BOC-piperazino)pyridine

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $28.00 $20.00 -   +
1g 97% in stock $30.00 $21.00 -   +
5g 97% in stock $124.00 $87.00 -   +
10g 97% in stock $212.00 $149.00 -   +
25g 97% in stock $418.00 $293.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA23804
Chemical Name: 5-Amino-2-(4-BOC-piperazino)pyridine
CAS Number: 119285-07-3
Molecular Formula: C14H22N4O2
Molecular Weight: 278.3501
MDL Number: MFCD05864841
SMILES: Nc1ccc(nc1)N1CCN(CC1)C(=O)OC(C)(C)C

 

Computed Properties
Complexity: 335  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 20  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 3  
XLogP3: 1.3  

 

 

Upstream Synthesis Route
  • The tert-Butyl 4-(5-aminopyridin-2-yl)piperazine-1-carboxylate is a versatile compound commonly utilized in chemical synthesis, particularly in the development of novel pharmaceuticals and organic compounds. Due to its unique structural properties, this compound serves as a key building block for the creation of various biologically active molecules within the field of medicinal chemistry.By incorporating tert-Butyl 4-(5-aminopyridin-2-yl)piperazine-1-carboxylate into synthetic pathways, chemists can introduce specific functional groups and stereochemical features that are crucial for enhancing the biological activity and pharmacokinetic profiles of the final products. This compound enables precise control over the molecular structure, leading to the production of new drug candidates with improved potency, selectivity, and safety profiles.In chemical synthesis, tert-Butyl 4-(5-aminopyridin-2-yl)piperazine-1-carboxylate plays a pivotal role as a strategic intermediate, facilitating the construction of complex molecular architectures through various synthetic transformations such as cross-coupling reactions, nucleophilic substitutions, and cyclization processes. Its compatibility with diverse synthetic methodologies makes it a valuable tool for designing and synthesizing advanced compounds for pharmaceutical applications.
FEATURED PRODUCTS