4-(N-BOC-amino)benzeneboronic acid
Pharmaceutical Materials 2025-03-20
CAS.No：380430-49-9
Appearance:White powder
Molecular Formula:C11H16BNO4
Purity:HPLC≥99.5%
Molecular weight:237.06
Application:20 tons/month
| Property | Details |
|---|---|
| Molecular Formula | C11H16BNO4 |
| Molecular Weight | 237.06 g/mol |
| Appearance | White to off-white crystalline solid or powder |
| Purity | Typically ≥95% |
| Melting Point | 220-225 °C (decomposition may occur) |
| Boiling Point | Predicted to be above 300 °C at 760 mmHg |
| Density | Approximately 1.2 g/cm³ (Predicted) |
| Solubility | Soluble in organic solvents such as DMSO, DMF, and methanol; slightly soluble in water |
| Applications | Organic synthesis, Suzuki-Miyaura coupling reactions, drug discovery, and biochemical research |
| Safety Considerations | Handle with care; avoid contact with skin and eyes; store in a cool, dry place away from moisture and strong acids |
| Suppliers | Available from specialized chemical suppliers |
Applications
4-(N-BOC-Amino)benzeneboronic acid is a versatile compound widely used in organic synthesis, particularly in Suzuki-Miyaura coupling reactions. Its boronic acid group and protected amine functionality provide unique reactivity, allowing for the formation of carbon-carbon bonds with various aryl and vinyl halides while maintaining the potential for further amine functionalization.
In drug discovery, this compound serves as a key intermediate in the synthesis of novel pharmaceutical compounds. The tert-butoxycarbonyl (BOC) protecting group can be easily removed under mild conditions, enabling the introduction of diverse amine functionalities. This flexibility makes 4-(N-BOC-Amino)benzeneboronic acid a valuable tool in the development of new therapeutic agents.
Its solubility in organic solvents facilitates its use in various synthetic methodologies, while its stability under appropriate storage conditions ensures its reliability in research and industrial applications. Additionally, this compound finds applications in biochemical research, where it is used to explore new chemical entities and biological pathways.
