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994-89-8

Tributylstannylacetylene

Catalog#: AR0036QV  |   CAS#: 994-89-8  |   MDL#: MFCD00009420  |   MF: C14H28Sn  |   MW: 315.0731

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1g 95% $4.00 Global Stock Buy Now Add To Cart
5g 95% $14.00 Global Stock Buy Now Add To Cart
10g 95% $25.00 Global Stock Buy Now Add To Cart
25g 95% $60.00 Global Stock Buy Now Add To Cart
50g 95% $118.00 Global Stock Buy Now Add To Cart
100g 95% $225.00 Global Stock Buy Now Add To Cart
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Catalog Number AR0036QV
Chemical Name Tributylstannylacetylene
CAS Number 994-89-8
Molecular Formula C14H28Sn
Molecular Weight 315.0731
MDL Number MFCD00009420
SMILES CCCC[Sn](C#C)(CCCC)CCCC
NSC Number 203201

Tributylstannylacetylene, a highly versatile organotin compound, serves as a valuable building block in chemical synthesis, particularly in the field of organic chemistry. Its unique structure and reactivity make it a popular choice for numerous applications, including:1. Cross-Coupling Reactions: Tributylstannylacetylene is commonly used as a coupling partner in Sonogashira cross-coupling reactions. This process involves the formation of carbon-carbon bonds and is widely employed in the synthesis of complex organic molecules.2. Functional Group Transformations: The acetylenic moiety in tributylstannylacetylene makes it a useful reagent for introducing alkynes into various chemical structures. This enables the selective functionalization of target molecules, offering a powerful tool for chemical transformations.3. Heterocycle Synthesis: Tributylstannylacetylene can participate in cycloaddition reactions to form heterocyclic compounds, such as pyrroles and furans. These heterocycles are essential building blocks in medicinal chemistry and material science.4. Polymer Chemistry: Due to its ability to undergo polymerization reactions, tributylstannylacetylene is used in the synthesis of polymeric materials with tailored properties. Its incorporation into polymer chains can impart specific functionalities and enhance material performance.Overall, tributylstannylacetylene plays a crucial role in diverse chemical synthesis strategies, offering synthetic chemists a versatile tool for constructing complex molecules and materials.
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