logo
Home  > Chemistry  > Heterocyclic Building Blocks  > Pyridines  > 2-Piperazinopyridine-5-boronic acid

AA01824

1003043-67-1 | 2-Piperazinopyridine-5-boronic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 96% in stock $43.00 $30.00 -   +
250mg 96% in stock $70.00 $49.00 -   +
1g 96% in stock $114.00 $80.00 -   +
10g 96% in stock $996.00 $697.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA01824
Chemical Name: 2-Piperazinopyridine-5-boronic acid
CAS Number: 1003043-67-1
Molecular Formula: C9H14BN3O2
Molecular Weight: 207.0374
MDL Number: MFCD11975410
SMILES: OB(c1ccc(nc1)N1CCNCC1)O

 

Computed Properties
Complexity: 200  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 3  
Rotatable Bond Count: 2  

 

 

Upstream Synthesis Route
  • The (6-(Piperazin-1-yl)pyridin-3-yl)boronic acid is a versatile compound that finds widespread application in chemical synthesis. Due to its boronic acid moiety, this compound acts as a key building block in the field of organic chemistry. Its unique structure and reactivity make it a valuable reagent for various transformations and reactions.One of the primary applications of (6-(Piperazin-1-yl)pyridin-3-yl)boronic acid is in Suzuki-Miyaura cross-coupling reactions. In this process, the boronic acid group allows for the formation of new carbon-carbon bonds, enabling the synthesis of complex organic molecules. This reaction is widely used in medicinal chemistry, material science, and other areas of chemical research.Additionally, the presence of the piperazine and pyridine motifs in the molecule provides additional opportunities for functionalization and derivatization. These functionalities can be further modified to introduce specific properties or reactivity into the target molecule, expanding the versatility of (6-(Piperazin-1-yl)pyridin-3-yl)boronic acid in the design and synthesis of novel compounds.Overall, (6-(Piperazin-1-yl)pyridin-3-yl)boronic acid serves as a valuable tool in the hands of synthetic chemists, allowing for the efficient construction of diverse molecular architectures with potential applications in drug discovery, materials science, and other scientific disciplines.
FEATURED PRODUCTS