Atomfair 5-(7-Bromobenzo[c][1,2,5]thiadiazol-4-yl)thiophene-2-carbaldehyde C11H5BrN2OS2

Description 5-(7-Bromobenzo[c][1,2,5]thiadiazol-4-yl)thiophene-2-carbaldehyde (CAS No. 1309922-61-9) is a high-purity heterocyclic organic compound with the molecular formula C11H5BrN2OS2. This specialized chemical features a benzo[c][1,2,5]thiadiazole core functionalized with a bromo substituent at the 7-position and a thiophene-2-carbaldehyde moiety at the 4-position. The compound is characterized by its unique electronic properties, making it valuable for advanced research in materials science and organic electronics. Supplied as a crystalline solid with ??95% purity (HPLC), it is ideal for use in cross-coupling reactions, polymer synthesis, and as a building block for optoelectronic materials. Proper storage at 2-8??C under inert atmosphere is recommended to maintain stability.

Description

Description

5-(7-Bromobenzo[c][1,2,5]thiadiazol-4-yl)thiophene-2-carbaldehyde (CAS No. 1309922-61-9) is a high-purity heterocyclic organic compound with the molecular formula C11H5BrN2OS2. This specialized chemical features a benzo[c][1,2,5]thiadiazole core functionalized with a bromo substituent at the 7-position and a thiophene-2-carbaldehyde moiety at the 4-position. The compound is characterized by its unique electronic properties, making it valuable for advanced research in materials science and organic electronics. Supplied as a crystalline solid with ??95% purity (HPLC), it is ideal for use in cross-coupling reactions, polymer synthesis, and as a building block for optoelectronic materials. Proper storage at 2-8??C under inert atmosphere is recommended to maintain stability.

  • CAS No: 1309922-61-9
  • Molecular Formula: C11H5BrN2OS2
  • Molecular Weight: 325.2
  • Exact Mass: 323.90267
  • Monoisotopic Mass: 323.90267
  • IUPAC Name: 5-(4-bromo-2,1,3-benzothiadiazol-7-yl)thiophene-2-carbaldehyde
  • SMILES: C1=C(SC(=C1)C2=CC=C(C3=NSN=C23)Br)C=O
  • Synonyms: 5-(7-bromobenzo[c][1,2,5]thiadiazol-4-yl)thiophene-2-carbaldehyde, 1309922-61-9, G66393, 2-Thiophenecarboxaldehyde,5-(7-bromo-2,1,3-benzothiadiazol-4-yl)-, 5-(4-bromo-2,1,3-benzothiadiazol-7-yl)thiophene-2-carbaldehyde

Application

This compound serves as a key intermediate in the synthesis of conjugated polymers and small molecules for organic electronics, particularly in the development of organic photovoltaics (OPVs) and light-emitting diodes (OLEDs). The bromo and aldehyde functional groups enable versatile reactivity for Suzuki coupling, Knoevenagel condensation, and other transformations. Researchers utilize it to construct donor-acceptor type materials with tailored optoelectronic properties. Its rigid ??-conjugated structure contributes to enhanced charge transport characteristics in semiconductor applications.

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