AB59392
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.
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 |
Complexity: | 184 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 18 |
Hydrogen Bond Acceptor Count: | 1 |
Rotatable Bond Count: | 10 |
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.