AA20174
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 95% | in stock | $42.00 | $30.00 | - + | |
1g | 95% | in stock | $108.00 | $76.00 | - + | |
5g | 95% | in stock | $323.00 | $226.00 | - + | |
25g | 95% | in stock | $1,317.00 | $922.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA20174 |
Chemical Name: | 2-(Pyrrolidinomethyl)phenylboronic acid, pinacol ester |
CAS Number: | 1150271-49-0 |
Molecular Formula: | C17H26BNO2 |
Molecular Weight: | 287.2048 |
MDL Number: | MFCD09746206 |
SMILES: | CC1(C)OB(OC1(C)C)c1ccccc1CN1CCCC1 |
Complexity: | 350 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 21 |
Hydrogen Bond Acceptor Count: | 3 |
Rotatable Bond Count: | 3 |
1-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)pyrrolidine plays a crucial role in chemical synthesis as a versatile building block. Its unique structure containing a boronate group makes it a valuable reagent for Suzuki-Miyaura cross-coupling reactions. This compound serves as an efficient ligand precursor for transition metal-catalyzed coupling reactions, allowing for the selective formation of complex organic molecules. Additionally, 1-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)pyrrolidine exhibits excellent stability and reactivity, making it an essential tool for the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The compound's ability to facilitate bond formation in a controlled manner under mild conditions highlights its significance in modern organic synthesis strategies.