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Home  > 2-(Tributylstannyl)furan

AB59392

118486-94-5 | 2-(Tributylstannyl)furan

Packsize Purity Availability Price Discounted Price    Quantity
1g 95% in stock $19.00 $13.00 -   +
25g 95% in stock $32.00 $23.00 -   +
100g 95% in stock $128.00 $90.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB59392
Chemical Name: 2-(Tributylstannyl)furan
CAS Number: 118486-94-5
Molecular Formula: C16H30OSn
Molecular Weight: 357.1098
MDL Number: MFCD00192512
SMILES: CCCC[Sn](c1ccco1)(CCCC)CCCC

 

Computed Properties
Complexity: 184  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 18  
Hydrogen Bond Acceptor Count: 1  
Rotatable Bond Count: 10  

 

 

Upstream Synthesis Route
  • Tributyl(furan-2-yl)stannane is a versatile organotin compound commonly used in chemical synthesis as a powerful reagent for various reactions. This unique compound plays a crucial role in organic synthesis due to its ability to facilitate carbon-carbon bond formation and functional group manipulation.In organic chemistry, Tributyl(furan-2-yl)stannane is often utilized as a reagent for Stille cross-coupling reactions. This reaction involves the coupling of two different organic groups, typically an organohalide and an organotin compound, to form a carbon-carbon bond. With its furan-2-yl group, this compound provides an added dimension of reactivity and selectivity to the Stille coupling process, leading to efficient bond formation and high product yields.Furthermore, Tributyl(furan-2-yl)stannane is also employed in the functionalization of organic molecules through radical reactions. The furan-2-yl group can serve as a radical acceptor, allowing for the controlled generation of radical intermediates that can participate in diverse transformation processes. This property makes Tributyl(furan-2-yl)stannane a valuable tool for the synthesis of complex organic molecules with specific functionalities.Overall, Tributyl(furan-2-yl)stannane is a key reagent in modern organic synthesis, enabling chemists to access a wide range of structurally diverse compounds through efficient and selective bond-forming reactions. Its versatile applications make it an indispensable component in the toolbox of synthetic chemists striving to develop novel molecules with tailored properties.
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