AA23625
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 95% | in stock | $267.00 | $187.00 | - + | |
250mg | 95% | in stock | $597.00 | $418.00 | - + | |
1g | 95% | in stock | $1,560.00 | $1,092.00 | - + | |
5g | 95% | in stock | $7,552.00 | $5,286.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA23625 |
Chemical Name: | 2-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-oxazole |
CAS Number: | 1192056-62-4 |
Molecular Formula: | C10H16BNO3 |
Molecular Weight: | 209.0499 |
MDL Number: | MFCD10697443 |
SMILES: | Cc1ncc(o1)B1OC(C(O1)(C)C)(C)C |
2-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)oxazole, commonly referred to as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in various organic reactions, particularly in the field of cross-coupling chemistry.One of the primary applications of 2-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)oxazole is as a boronic ester reagent in palladium-catalyzed cross-coupling reactions. This compound serves as a valuable substrate for Suzuki-Miyaura coupling reactions, enabling the formation of carbon-carbon bonds in a selective and efficient manner. The presence of the boronic ester group allows for the introduction of functionalized aryl or heteroaryl groups into a desired molecular scaffold, making it an essential building block in the synthesis of complex organic molecules.Furthermore, the unique structure of 2-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)oxazole imparts enhanced stability and reactivity, making it a preferred choice for chemists involved in the development of pharmaceuticals, agrochemicals, and materials science. Its compatibility with a wide range of substrates and reaction conditions further enhances its utility in modern organic synthesis.In summary, 2-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)oxazole is a key reagent in chemical synthesis, particularly in palladium-catalyzed cross-coupling reactions, offering chemists an invaluable tool for the construction of complex organic molecules with high precision and efficiency.