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Home  > Chemistry  > Heterocyclic Building Blocks  > Furans  > 4,5-Dihydrofuran-3-boronic acid pinacol ester

AB66338

1046812-03-6 | 4,5-Dihydrofuran-3-boronic acid pinacol ester

Packsize Purity Availability Price Discounted Price    Quantity
50mg 96% in stock $36.00 $25.00 -   +
100mg 96% in stock $45.00 $32.00 -   +
250mg 96% in stock $92.00 $65.00 -   +
1g 96% in stock $290.00 $203.00 -   +
25g 96% in stock $5,609.00 $3,927.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB66338
Chemical Name: 4,5-Dihydrofuran-3-boronic acid pinacol ester
CAS Number: 1046812-03-6
Molecular Formula: C10H17BO3
Molecular Weight: 196.0512
MDL Number: MFCD13182120
SMILES: CC1(C)OB(OC1(C)C)C1=COCC1

 

Computed Properties
Complexity: 255  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 14  
Hydrogen Bond Acceptor Count: 3  
Rotatable Bond Count: 1  

 

 

Upstream Synthesis Route
  • 2-(4,5-Dihydrofuran-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile compound that finds widespread application in chemical synthesis. This unique compound serves as a valuable building block in organic chemistry, particularly in the field of organic synthesis and pharmaceutical research. Due to its reactive boron functionality, it acts as a key reagent for the direct introduction of a tetramethylaryl group into various organic molecules. This enables the construction of complex molecular structures with high efficiency and precision.In addition, 2-(4,5-Dihydrofuran-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is commonly employed in cross-coupling reactions, a fundamental strategy in modern organic chemistry for the formation of carbon-carbon bonds. Through Suzuki-Miyaura coupling and other similar transformations, this compound facilitates the synthesis of biaryl compounds, heterocycles, natural products, and pharmaceutical intermediates. Its unique combination of boron and furan functionalities imparts specific reactivity and selectivity, making it a valuable tool for chemists to access diverse molecular scaffolds efficiently.Overall, the application of 2-(4,5-Dihydrofuran-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane in chemical synthesis represents a powerful approach to streamline the construction of complex organic molecules, offering tremendous potential for innovation and discovery in synthetic chemistry.
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