AA01824
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.
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 |
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 |
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.