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AA54565

1218790-71-6 | 4-Formyl-3,5-dimethylphenylboronic acid

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $74.00 $52.00 -   +
1g 97% in stock $161.00 $113.00 -   +
5g 97% in stock $605.00 $423.00 -   +
10g 97% in stock $1,132.00 $793.00 -   +
25g 97% in stock $2,314.00 $1,620.00 -   +

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*All prices are in USD.

Description
Catalog Number: AA54565
Chemical Name: 4-Formyl-3,5-dimethylphenylboronic acid
CAS Number: 1218790-71-6
Molecular Formula: C9H11BO3
Molecular Weight: 177.9928
MDL Number: MFCD15143475
SMILES: O=Cc1c(C)cc(cc1C)B(O)O

 

Computed Properties
Complexity: 172  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 2  

 

 

Upstream Synthesis Route
  • (4-Formyl-3,5-dimethylphenyl)boronic acid, also known as $name$, is a versatile compound commonly used in organic chemical synthesis. This compound serves as a key building block in the preparation of various functionalized materials and pharmaceutical intermediates.In chemical synthesis, (4-Formyl-3,5-dimethylphenyl)boronic acid plays a crucial role as a mild and selective reagent for the formation of carbon-carbon and carbon-heteroatom bonds. It is frequently employed in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronate ester partner to react with various aryl and heteroaryl halides under mild conditions. This reaction is widely utilized in the synthesis of complex organic molecules, including natural products and pharmaceuticals.Additionally, (4-Formyl-3,5-dimethylphenyl)boronic acid can also participate in other types of transformations such as Chan-Lam coupling, borylation reactions, and C-H activation processes. Its ability to introduce the formyl group and boronic acid functionality into organic molecules makes it a valuable reagent for the construction of diverse chemical structures with high efficiency and selectivity.Overall, the application of (4-Formyl-3,5-dimethylphenyl)boronic acid in chemical synthesis enables the rapid and controlled construction of complex organic compounds, making it an essential tool for organic chemists and researchers in the field.
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