AE20048
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 96% | in stock | $105.00 | $74.00 | - + | |
5g | 96% | in stock | $293.00 | $205.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AE20048 |
Chemical Name: | 4-(Hydroxy(thiazol-2-yl)methyl)phenylboronic acid, pinacol ester |
CAS Number: | 1073371-73-9 |
Molecular Formula: | C16H20BNO3S |
Molecular Weight: | 317.2109 |
MDL Number: | MFCD09953504 |
SMILES: | OC(c1nccs1)c1ccc(cc1)B1OC(C(O1)(C)C)(C)C |
Complexity: | 383 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 22 |
Hydrogen Bond Acceptor Count: | 5 |
Hydrogen Bond Donor Count: | 1 |
Rotatable Bond Count: | 3 |
Undefined Atom Stereocenter Count: | 1 |
The compound (4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)(thiazol-2-yl)methanol, commonly referred to as $name$, is a versatile reagent that plays a crucial role in chemical synthesis. This compound is primarily utilized as a key building block in the development of various organic molecules due to its unique structural properties and reactivity.One of the key applications of $name$ in chemical synthesis is as a boronic ester reagent in Suzuki-Miyaura cross-coupling reactions. In this process, $name$ acts as a boron source that undergoes transmetallation with an organoboron compound in the presence of a palladium catalyst. This reaction allows for the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules with high selectivity and efficiency.Moreover, the thiazole moiety in $name$ confers additional functionality and diversity to the synthesized molecules, making it a valuable tool in medicinal chemistry and material science. The combination of boronic ester and thiazole functionalities in $name$ offers a wide range of synthetic possibilities, allowing chemists to access novel compounds with tailored properties and applications.Overall, the strategic incorporation of (4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)(thiazol-2-yl)methanol in chemical synthesis enables the streamlined and efficient construction of complex molecules, making it an indispensable reagent in modern organic chemistry research.