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AB65318

1073354-66-1 | 4-Formyl-2-methylphenylboronic acid pinacol ester

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.

Description
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

 

Computed Properties
Complexity: 311  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 18  
Hydrogen Bond Acceptor Count: 3  
Rotatable Bond Count: 2  

 

 

Upstream Synthesis Route
  • 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.
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