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Atomfair Tributyl(1-methoxyethenyl)stannane C15H32OSn

Description Tributyl(1-methoxyethenyl)stannane (CAS No. 81177-90-4) is a highly specialized organotin compound with the molecular formula C15H32OSn . This reagent is widely utilized in organic synthesis, particularly in Stille coupling reactions, due to its ability to transfer the 1-methoxyethenyl group to various electrophilic partners. Its high purity and stability make it an essential tool for researchers in pharmaceuticals, materials science, and catalysis. The compound is supplied as a clear to pale yellow liquid and should be stored under inert conditions to prevent degradation. Suitable for use in anhydrous reactions, it offers excellent reactivity and selectivity for advanced synthetic applications.

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Description

Description

Tributyl(1-methoxyethenyl)stannane (CAS No. 81177-90-4) is a highly specialized organotin compound with the molecular formula C15H32OSn. This reagent is widely utilized in organic synthesis, particularly in Stille coupling reactions, due to its ability to transfer the 1-methoxyethenyl group to various electrophilic partners. Its high purity and stability make it an essential tool for researchers in pharmaceuticals, materials science, and catalysis. The compound is supplied as a clear to pale yellow liquid and should be stored under inert conditions to prevent degradation. Suitable for use in anhydrous reactions, it offers excellent reactivity and selectivity for advanced synthetic applications.

  • CAS No: 81177-90-4
  • Molecular Formula: C15H32OSn
  • Molecular Weight: 347.12
  • Exact Mass: 348.147518
  • Monoisotopic Mass: 348.147518
  • IUPAC Name: tributyl(1-methoxyethenyl)stannane
  • SMILES: CCCC[Sn](CCCC)(CCCC)C(=C)OC
  • Synonyms: 81177-90-4, TRIBUTYL(1-METHOXYETHENYL)STANNANE, DTXSID80510778, DTXCID90461585, 837-963-9

Application

Tributyl(1-methoxyethenyl)stannane is primarily used in Stille cross-coupling reactions to introduce the 1-methoxyethenyl moiety into complex organic molecules. It is valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Researchers also employ it in the preparation of vinyl ether derivatives and as a building block for functionalized polymers. Its stability and reactivity make it ideal for controlled, selective transformations under mild conditions.

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