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Atomfair Tributyl(3-hexylthiophen-2-yl)stannane C22H42SSn

Description Tributyl(3-hexylthiophen-2-yl)stannane (CAS No. 851853-51-5) is a high-purity organotin compound with the molecular formula C22H42SSn . This specialized reagent is widely utilized in organic synthesis, particularly in Stille coupling reactions, due to its excellent reactivity and stability. The compound features a hexyl-substituted thiophene moiety coupled with a tributylstannane group, making it ideal for constructing conjugated polymers and advanced materials. Suitable for research and industrial applications, this product is rigorously tested to ensure superior quality, consistency, and performance. Packaged under inert conditions to maintain stability, it is an essential tool for synthetic chemists and material scientists.

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Description

Description

Tributyl(3-hexylthiophen-2-yl)stannane (CAS No. 851853-51-5) is a high-purity organotin compound with the molecular formula C22H42SSn. This specialized reagent is widely utilized in organic synthesis, particularly in Stille coupling reactions, due to its excellent reactivity and stability. The compound features a hexyl-substituted thiophene moiety coupled with a tributylstannane group, making it ideal for constructing conjugated polymers and advanced materials. Suitable for research and industrial applications, this product is rigorously tested to ensure superior quality, consistency, and performance. Packaged under inert conditions to maintain stability, it is an essential tool for synthetic chemists and material scientists.

  • CAS No: 851853-51-5
  • Molecular Formula: C22H42SSn
  • Molecular Weight: 457.3
  • Exact Mass: 458.202925
  • Monoisotopic Mass: 458.202925
  • IUPAC Name: tributyl-(3-hexylthiophen-2-yl)stannane
  • SMILES: CCCCCCC1=C(SC=C1)[Sn](CCCC)(CCCC)CCCC
  • Synonyms: SCHEMBL2566044, Tributyl(3-hexylthiophen-2-yl)stannane, 851853-51-5

Application

Tributyl(3-hexylthiophen-2-yl)stannane is primarily used in Stille cross-coupling reactions to synthesize conjugated polymers and small molecules for organic electronics. Its application extends to the development of organic photovoltaics (OPVs), field-effect transistors (OFETs), and light-emitting diodes (OLEDs). The hexylthiophene moiety enhances solubility and processability in organic solvents, facilitating thin-film fabrication. Researchers value this compound for its reliability in constructing complex ??-conjugated systems with tailored optoelectronic properties.

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