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Atomfair 4,4′-Dibutoxy-2,2′-bis(trimethylstannyl)-5,5′-bithiazole DPP1014-2Br C20H36N2O2S2Sn2

Description 4,4′-Dibutoxy-2,2′-bis(trimethylstannyl)-5,5′-bithiazole (CAS No. 2432086-16-1) is a highly specialized organotin compound with the molecular formula C20H36N2O2S2Sn2. This advanced chemical features a bithiazole core functionalized with butoxy groups and trimethylstannyl moieties, making it a valuable precursor for metal-organic frameworks (MOFs), conjugated polymers, and organic electronics. Its precise IUPAC name is [4-butoxy-5-(4-butoxy-2-trimethylstannyl-1,3-thiazol-5-yl)-1,3-thiazol-2-yl]-trimethylstannane . The compound is supplied as a high-purity solid (>95%) with strict quality control to ensure consistency in sensitive applications. Store under inert conditions to prevent degradation.

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Description

Description

4,4′-Dibutoxy-2,2′-bis(trimethylstannyl)-5,5′-bithiazole (CAS No. 2432086-16-1) is a highly specialized organotin compound with the molecular formula C20H36N2O2S2Sn2. This advanced chemical features a bithiazole core functionalized with butoxy groups and trimethylstannyl moieties, making it a valuable precursor for metal-organic frameworks (MOFs), conjugated polymers, and organic electronics. Its precise IUPAC name is [4-butoxy-5-(4-butoxy-2-trimethylstannyl-1,3-thiazol-5-yl)-1,3-thiazol-2-yl]-trimethylstannane. The compound is supplied as a high-purity solid (>95%) with strict quality control to ensure consistency in sensitive applications. Store under inert conditions to prevent degradation.

  • CAS No: 2432086-16-1
  • Molecular Formula: C20H36N2O2S2Sn2
  • Molecular Weight: 638.1
  • Exact Mass: 638.02563
  • Monoisotopic Mass: 640.02623
  • IUPAC Name: [4-butoxy-5-(4-butoxy-2-trimethylstannyl-1,3-thiazol-5-yl)-1,3-thiazol-2-yl]-trimethylstannane
  • SMILES: CCCCOC1=C(SC(=N1)[Sn](C)(C)C)C2=C(N=C(S2)[Sn](C)(C)C)OCCCC
  • Synonyms: 4,4′-Dibutoxy-2,2′-bis(trimethylstannyl)-5,5′-bithiazole, DPP1014-2Br, 2432086-16-1

Application

This stannylated bithiazole derivative is primarily used in Stille coupling reactions to synthesize conjugated polymers for organic photovoltaics (OPVs) and field-effect transistors (OFETs). Its dual stannyl groups enable efficient cross-coupling with aryl halides, facilitating the construction of extended ??-systems. Researchers also employ it as a building block for near-infrared (NIR) emitters and electroluminescent materials in OLED development. The butoxy side chains enhance solubility for solution-processable device fabrication.

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