AB55229
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 98% | in stock | $163.00 | $114.00 | - + | |
1g | 98% | in stock | $299.00 | $209.00 | - + | |
5g | 98% | in stock | $1,132.00 | $793.00 | - + | |
10g | 98% | in stock | $1,879.00 | $1,316.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB55229 |
Chemical Name: | 5-((Boc-Amino)methyl)furan-2-boronic acid |
CAS Number: | 1072946-49-6 |
Molecular Formula: | C10H16BNO5 |
Molecular Weight: | 241.0487 |
MDL Number: | MFCD11053783 |
SMILES: | OB(c1ccc(o1)CNC(=O)OC(C)(C)C)O |
Complexity: | 266 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 17 |
Hydrogen Bond Acceptor Count: | 5 |
Hydrogen Bond Donor Count: | 3 |
Rotatable Bond Count: | 5 |
The compound $name$ (5-(((tert-Butoxycarbonyl)amino)methyl)furan-2-yl)boronic acid) plays a crucial role in chemical synthesis as a versatile building block. With its boronic acid group, this molecule serves as a valuable reagent in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. By coupling with various aryl or vinyl halides under palladium catalysis, $name$ enables the efficient synthesis of complex organic molecules. Furthermore, the presence of the furan ring in $name$ can participate in Diels-Alder reactions, providing a platform for constructing diverse heterocyclic structures. Its tert-butoxycarbonyl-protected amine moiety also offers a means of introducing amino functionalities into target molecules, expanding the synthetic possibilities of this versatile compound.