Atomfair (4-(Bis(4-(hexyloxy)phenyl)amino)phenyl)boronic acid C30H40BNO4

Description (4-(Bis(4-(hexyloxy)phenyl)amino)phenyl)boronic acid (CAS No. 1380786-94-6) is a high-purity boronic acid derivative designed for advanced research applications. With the molecular formula C30H40BNO4, this compound features a unique triarylamine core functionalized with hexyloxy chains and a terminal boronic acid group, making it an excellent candidate for organic electronics, supramolecular chemistry, and cross-coupling reactions. Its IUPAC name, [4-(4-hexoxy-N-(4-hexoxyphenyl)anilino)phenyl]boronic acid , reflects its precise structural configuration. This product is synthesized under stringent quality controls to ensure consistency, and it is provided as a solid with >95% purity (HPLC). Ideal for researchers developing OLED materials, sensors, or catalysts, this compound offers exceptional solubility in…

Description

Description

(4-(Bis(4-(hexyloxy)phenyl)amino)phenyl)boronic acid (CAS No. 1380786-94-6) is a high-purity boronic acid derivative designed for advanced research applications. With the molecular formula C30H40BNO4, this compound features a unique triarylamine core functionalized with hexyloxy chains and a terminal boronic acid group, making it an excellent candidate for organic electronics, supramolecular chemistry, and cross-coupling reactions. Its IUPAC name, [4-(4-hexoxy-N-(4-hexoxyphenyl)anilino)phenyl]boronic acid, reflects its precise structural configuration. This product is synthesized under stringent quality controls to ensure consistency, and it is provided as a solid with >95% purity (HPLC). Ideal for researchers developing OLED materials, sensors, or catalysts, this compound offers exceptional solubility in common organic solvents like THF, DCM, and toluene. Store under inert conditions at 2-8??C to maintain stability.

  • CAS No: 1380786-94-6
  • Molecular Formula: C30H40BNO4
  • Molecular Weight: 489.5
  • Exact Mass: 489.3050389
  • Monoisotopic Mass: 489.3050389
  • IUPAC Name: [4-(4-hexoxy-N-(4-hexoxyphenyl)anilino)phenyl]boronic acid
  • SMILES: B(C1=CC=C(C=C1)N(C2=CC=C(C=C2)OCCCCCC)C3=CC=C(C=C3)OCCCCCC)(O)O
  • Synonyms: (4-(Bis(4-(hexyloxy)phenyl)amino)phenyl)boronic acid, 1380786-94-6

Application

This boronic acid derivative is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to construct conjugated polymers for optoelectronic devices. Its triarylamine backbone makes it valuable in OLED and OFET research as a hole-transporting material. Researchers also employ it in molecular recognition systems due to the boronic acid’s affinity for diols, enabling applications in glucose sensing or glycoprotein analysis.

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