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Atomfair Didecyl 5,5”-dibromo-[2,2′:5′,2”-terthiophene]-3,3”-dicarboxylate C34H46Br2O4S3

Description Didecyl 5,5”-dibromo-[2,2′:5′,2”-terthiophene]-3,3”-dicarboxylate (CAS: 2567035-56-5) is a high-purity, synthetic organic compound with the molecular formula C34H46Br2O4S3. This terthiophene derivative features dibromo substitution and didecyl ester functionalization, making it a valuable building block for advanced materials research. The compound exhibits excellent solubility in common organic solvents, facilitating its use in solution-phase processing. With a molecular weight of 766.72 g/mol, this product is supplied as a solid with >95% purity (HPLC), ensuring consistency for demanding applications. Its extended ??-conjugated system and brominated termini make it particularly suitable for cross-coupling reactions in the synthesis of conjugated polymers and small molecules. Ideal for researchers…

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Description

Description

Didecyl 5,5”-dibromo-[2,2′:5′,2”-terthiophene]-3,3”-dicarboxylate (CAS: 2567035-56-5) is a high-purity, synthetic organic compound with the molecular formula C34H46Br2O4S3. This terthiophene derivative features dibromo substitution and didecyl ester functionalization, making it a valuable building block for advanced materials research. The compound exhibits excellent solubility in common organic solvents, facilitating its use in solution-phase processing. With a molecular weight of 766.72 g/mol, this product is supplied as a solid with >95% purity (HPLC), ensuring consistency for demanding applications. Its extended ??-conjugated system and brominated termini make it particularly suitable for cross-coupling reactions in the synthesis of conjugated polymers and small molecules. Ideal for researchers developing organic semiconductors, photovoltaic materials, or electroactive polymers.

  • CAS No: 2567035-56-5
  • Molecular Formula: C34H46Br2O4S3
  • Molecular Weight: 774.7
  • Exact Mass: 774.09045
  • Monoisotopic Mass: 772.09250
  • IUPAC Name: decyl 5-bromo-2-[5-(5-bromo-3-decoxycarbonylthiophen-2-yl)thiophen-2-yl]thiophene-3-carboxylate
  • SMILES: CCCCCCCCCCOC(=O)C1=C(SC(=C1)Br)C2=CC=C(S2)C3=C(C=C(S3)Br)C(=O)OCCCCCCCCCC
  • Synonyms: Didecyl 5,5”-dibromo-[2,2′:5′,2”-terthiophene]-3,3”-dicarboxylate, 2567035-56-5

Application

This dibromo-terthiophene derivative serves as a key monomer in the synthesis of conjugated polymers for organic electronic applications. It is particularly useful in the development of donor-acceptor copolymers for organic photovoltaics and field-effect transistors. The bromine substituents enable efficient cross-coupling reactions in palladium-catalyzed polymerizations. Researchers also utilize this compound as a building block for creating electrochromic materials and conductive polymers. Its extended conjugation makes it valuable for studying charge transport mechanisms in organic semiconductors.

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