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Atomfair 4-[4-[4-(4-methoxy-N-(4-methoxyphenyl)anilino)phenyl]-2,1,3-benzothiadiazol-7-yl]benzoic acid C33H25N3O4S

Description 4-[4-[4-(4-methoxy-N-(4-methoxyphenyl)anilino)phenyl]-2,1,3-benzothiadiazol-7-yl]benzoic acid (CAS: 2810129-76-9) is a high-purity organic compound with the molecular formula C33H25N3O4S . This advanced chemical features a benzothiadiazole core functionalized with a benzoic acid moiety and bis(4-methoxyphenyl)amino groups, making it a valuable building block for optoelectronic and materials science research. The compound exhibits strong electron-accepting properties due to its conjugated structure and is particularly useful in the development of organic semiconductors, dye-sensitized solar cells (DSSCs), and fluorescent probes. With a molecular weight of 559.64 g/mol, this product is supplied as a solid with guaranteed ??95% purity (HPLC) and is rigorously characterized by1H NMR,13C NMR, and mass…

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Description

Description

4-[4-[4-(4-methoxy-N-(4-methoxyphenyl)anilino)phenyl]-2,1,3-benzothiadiazol-7-yl]benzoic acid (CAS: 2810129-76-9) is a high-purity organic compound with the molecular formula C33H25N3O4S. This advanced chemical features a benzothiadiazole core functionalized with a benzoic acid moiety and bis(4-methoxyphenyl)amino groups, making it a valuable building block for optoelectronic and materials science research. The compound exhibits strong electron-accepting properties due to its conjugated structure and is particularly useful in the development of organic semiconductors, dye-sensitized solar cells (DSSCs), and fluorescent probes. With a molecular weight of 559.64 g/mol, this product is supplied as a solid with guaranteed ??95% purity (HPLC) and is rigorously characterized by 1H NMR, 13C NMR, and mass spectrometry. Proper storage at 2-8??C under inert atmosphere is recommended to maintain stability.

  • CAS No: 2810129-76-9
  • Molecular Formula: C33H25N3O4S
  • Molecular Weight: 559.6
  • Exact Mass: 559.15657746
  • Monoisotopic Mass: 559.15657746
  • IUPAC Name: 4-[4-[4-(4-methoxy-N-(4-methoxyphenyl)anilino)phenyl]-2,1,3-benzothiadiazol-7-yl]benzoic acid
  • SMILES: COC1=CC=C(C=C1)N(C2=CC=C(C=C2)C3=CC=C(C4=NSN=C34)C5=CC=C(C=C5)C(=O)O)C6=CC=C(C=C6)OC
  • Synonyms: 2810129-76-9, DB-380463, 4-[7-[4-[Bis(4-methoxyphenyl)amino]phenyl]-2,1,3-benzothiadiazol-4-yl]benzoic acid

Application

This compound serves as a key intermediate in the synthesis of advanced organic electronic materials, particularly for use in photovoltaic devices and OLEDs. Its extended ??-conjugation and electron-deficient benzothiadiazole unit make it ideal for developing high-performance donor-acceptor type polymers. Researchers utilize this material to study charge transport mechanisms in thin-film transistors and as a fluorescent marker in bioimaging applications. The carboxylic acid functionality allows for further derivatization or anchoring to metal oxide surfaces in DSSCs.

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