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Atomfair N,N-diphenyl-4-(7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[c][1,2,5]thiadiazol-4-yl)aniline C30H28BN3O2S

Description N,N-diphenyl-4-(7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[c][1,2,5]thiadiazol-4-yl)aniline (CAS: 1883615-46-0) is a high-purity boronate ester derivative featuring a benzothiadiazole core, designed for advanced research and synthetic applications. With the molecular formula C30H28BN3O2S , this compound exhibits exceptional stability and reactivity, making it ideal for cross-coupling reactions such as Suzuki-Miyaura couplings. The presence of both electron-rich diphenylaniline and electron-deficient benzothiadiazole moieties enables tunable optoelectronic properties, suitable for organic electronics and material science research. This product is rigorously characterized by NMR, HPLC, and mass spectrometry to ensure ??95% purity, meeting the stringent demands of academic and industrial researchers.

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Description

Description

N,N-diphenyl-4-(7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[c][1,2,5]thiadiazol-4-yl)aniline (CAS: 1883615-46-0) is a high-purity boronate ester derivative featuring a benzothiadiazole core, designed for advanced research and synthetic applications. With the molecular formula C30H28BN3O2S, this compound exhibits exceptional stability and reactivity, making it ideal for cross-coupling reactions such as Suzuki-Miyaura couplings. The presence of both electron-rich diphenylaniline and electron-deficient benzothiadiazole moieties enables tunable optoelectronic properties, suitable for organic electronics and material science research. This product is rigorously characterized by NMR, HPLC, and mass spectrometry to ensure ??95% purity, meeting the stringent demands of academic and industrial researchers.

  • CAS No: 1883615-46-0
  • Molecular Formula: C30H28BN3O2S
  • Molecular Weight: 505.4
  • Exact Mass: 505.1995285
  • Monoisotopic Mass: 505.1995285
  • IUPAC Name: N,N-diphenyl-4-[7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,1,3-benzothiadiazol-4-yl]aniline
  • SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC=C(C3=NSN=C23)C4=CC=C(C=C4)N(C5=CC=CC=C5)C6=CC=CC=C6
  • Synonyms: 1883615-46-0, N,N-diphenyl-4-(7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[c][1,2,5]thiadiazol-4-yl)aniline

Application

This compound serves as a key intermediate in the synthesis of organic semiconductors, OLEDs, and photovoltaic materials due to its boronate ester functionality and conjugated structure. Researchers utilize it in Suzuki-Miyaura cross-coupling reactions to construct extended ??-systems for optoelectronic devices. Its benzothiadiazole core also makes it valuable in developing fluorescent probes and sensors for biochemical applications.

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