Hexabutylditin (CAS 813-19-4): A Versatile Reagent for Organic Synthesis and Chemical Innovations

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Advantages of Hexabutylditin

Enhanced Synthetic Pathways

Hexabutylditin facilitates advanced palladium-catalyzed tin-carbon bond formation, opening doors to novel molecular architectures and efficient synthetic routes.

Versatile Reaction Capabilities

The compound excels in deoxygenation and desulfurization reactions, demonstrating its broad applicability across different chemical transformations and industries.

Radical Chemistry Precision

As a key tributylstannyl radical source, Hexabutylditin allows for controlled radical reactions, crucial for stereoselective synthesis and complex molecule assembly.

Key Applications

Organic Synthesis

Hexabutylditin is essential for various organic synthesis procedures, particularly those involving organometallic intermediates and carbon-carbon bond formation.

Catalysis

Its role in palladium-catalyzed reactions highlights its importance as a co-catalyst or reagent in promoting efficient chemical transformations.

Stille Coupling

Hexabutylditin serves as a critical reagent for Stille coupling, a widely used cross-coupling reaction for forming carbon-carbon bonds with organostannanes.

Radioiodination

The compound finds specific use in the radioiodination of styrlpyridines, an important process in radiochemistry and medical imaging applications.