AB77042
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
500mg | 98% | in stock | $19.00 | $13.00 | - + | |
5g | 98% | in stock | $131.00 | $92.00 | - + | |
25g | 98% | in stock | $480.00 | $336.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB77042 |
Chemical Name: | 4-(N-Benzylaminocarbonyl)phenylboronic acid, pinacol ester |
CAS Number: | 1073353-57-7 |
Molecular Formula: | C20H24BNO3 |
Molecular Weight: | 337.2205 |
MDL Number: | MFCD09266184 |
SMILES: | O=C(c1ccc(cc1)B1OC(C(O1)(C)C)(C)C)NCc1ccccc1 |
Complexity: | 450 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 25 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 1 |
Rotatable Bond Count: | 4 |
N-Benzyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide is a versatile compound that finds widespread utility in chemical synthesis processes. In organic chemistry, it serves as a valuable building block for the construction of complex molecules due to its unique structural features. This compound is particularly prized for its ability to undergo selective functional group transformations, making it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and materials science. Additionally, the presence of the boron moiety in this molecule enables it to participate in various cross-coupling reactions, further expanding its synthetic possibilities. Its strategic placement of functional groups provides chemists with opportunities for site-selective modifications, facilitating the creation of diverse molecular scaffolds with high precision.