AB65318
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 98% | in stock | $55.00 | $38.00 | - + | |
1g | 98% | in stock | $145.00 | $102.00 | - + | |
5g | 98% | in stock | $511.00 | $358.00 | - + |
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*All prices are in USD.
Catalog Number: | AB65318 |
Chemical Name: | 4-Formyl-2-methylphenylboronic acid pinacol ester |
CAS Number: | 1073354-66-1 |
Molecular Formula: | C14H19BO3 |
Molecular Weight: | 246.1099 |
MDL Number: | MFCD08669583 |
SMILES: | O=Cc1ccc(c(c1)C)B1OC(C(O1)(C)C)(C)C |
Complexity: | 311 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 18 |
Hydrogen Bond Acceptor Count: | 3 |
Rotatable Bond Count: | 2 |
3-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde, a specialized compound in chemical synthesis, serves as a valuable building block in the creation of complex organic molecules. Its unique structure, featuring a boronic ester and aldehyde functional groups, enables it to participate in a variety of important reactions, particularly in the field of organic chemistry.One significant application of 3-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde lies in the Suzuki-Miyaura cross-coupling reaction, a powerful tool for the formation of carbon-carbon bonds. In this process, the boronic ester moiety of the compound undergoes a palladium-catalyzed coupling with an aryl halide or pseudohalide, leading to the formation of a new carbon-carbon bond. This reaction is widely used in the synthesis of pharmaceuticals, agrochemicals, and materials science.Furthermore, the aldehyde group in 3-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde can participate in various transformations, such as nucleophilic addition reactions, enabling the introduction of additional functional groups or further derivatization of the molecule. This versatility makes the compound a valuable intermediate in the synthesis of more complex organic compounds.Overall, the strategic placement of both boronic ester and aldehyde functional groups in 3-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde makes it a versatile and indispensable tool in chemical synthesis, facilitating the construction of diverse organic molecules with potential applications in various industries.