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AA53950

1217501-34-2 | 4-(Propylsulfonyl)phenylboronic acid

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $96.00 $67.00 -   +
1g 98% in stock $137.00 $96.00 -   +
5g 98% in stock $386.00 $270.00 -   +
25g 98% in stock $1,131.00 $792.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA53950
Chemical Name: 4-(Propylsulfonyl)phenylboronic acid
CAS Number: 1217501-34-2
Molecular Formula: C9H13BO4S
Molecular Weight: 228.0731
MDL Number: MFCD13195655
SMILES: CCCS(=O)(=O)c1ccc(cc1)B(O)O

 

Computed Properties
Complexity: 275  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 4  

 

 

Upstream Synthesis Route
  • (4-(Propylsulfonyl)phenyl)boronic acid is a versatile chemical reagent commonly utilized in organic synthesis as a key building block. With its unique structure and properties, this compound plays a crucial role in various chemical transformations and reactions. In the realm of synthetic chemistry, it serves as a valuable tool for creating complex molecular structures and functional materials. The presence of the boronic acid functional group enables (4-(Propylsulfonyl)phenyl)boronic acid to participate in Suzuki coupling reactions, where it forms carbon-carbon bonds with aryl halides or vinyl halides under palladium catalysis. This reaction is widely employed in the synthesis of pharmaceuticals, agrochemicals, and materials science. Additionally, the sulfonyl group in (4-(Propylsulfonyl)phenyl)boronic acid imparts unique physicochemical properties, making it a useful component in designing advanced organic molecules. Furthermore, this compound can be used for the construction of diverse molecular scaffolds and building blocks, facilitating the creation of novel compounds with potential applications in drug discovery, materials science, and chemical biology. Overall, (4-(Propylsulfonyl)phenyl)boronic acid stands as a valuable reagent in the arsenal of synthetic chemists, enabling the efficient and controlled synthesis of intricate organic molecules with tailored properties and functionalities.
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