AE18526
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 98% | in stock | $23.00 | $17.00 | - + | |
250mg | 98% | in stock | $41.00 | $29.00 | - + | |
1g | 98% | in stock | $103.00 | $73.00 | - + | |
5g | 98% | in stock | $435.00 | $305.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AE18526 |
Chemical Name: | 2-Methoxypyrimidin-5-ylboronic acid pinacol ester |
CAS Number: | 1052686-60-8 |
Molecular Formula: | C11H17BN2O3 |
Molecular Weight: | 236.0753 |
MDL Number: | MFCD13182190 |
SMILES: | COc1ncc(cn1)B1OC(C(O1)(C)C)(C)C |
Complexity: | 262 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 17 |
Hydrogen Bond Acceptor Count: | 5 |
Rotatable Bond Count: | 2 |
2-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine is a valuable reagent widely utilized in chemical synthesis for the functionalization of organic compounds. This compound serves as a key building block in various reactions due to its unique structural properties and versatile reactivity. In particular, it is commonly employed in Suzuki-Miyaura cross-coupling reactions, where it acts as a boron-containing coupling partner to form biaryl compounds. Additionally, 2-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine is used in the synthesis of pharmaceuticals, agrochemicals, materials, and other fine chemicals. Its ability to facilitate the formation of carbon-carbon bonds through palladium-catalyzed cross-coupling reactions makes it an indispensable tool for organic chemists seeking to access diverse molecular structures with high precision and efficiency.