2,5-Bis(5-tert-butylbenzooxazol-2-yl)thiophene

• CAT Number: R022929
• CAS Number: 7128-64-5
• Molecular Formula: C26H26N2O2S
• Molecular Weight: 430.57
• Purity: ≥95%
• Synonyms: 2,2’-(2,5-Thiophenediyl)bis[5-(1,1-dimethylethyl)]-benzoxazole;?2,2’-(2,5-Thiophenediyl)bis(5-tert-butyl)-benzoxazole; 2,2’-(2,5-Thiophenediyl)bis[5-(1,1-dimethylethyl)]benzoxazole; 2,2’-(2,5-Thiophenediyl)bis[5-tert-butylbenzoxazole]; 2,5-Bis(5-tert
• Storage: -20°C
• IUPAC Name: 5-tert-butyl-2-[5-(5-tert-butyl-1,3-benzoxazol-2-yl)thiophen-2-yl]-1,3-benzoxazole
• InChI: InChI=1S/C26H26N2O2S/c1-25(2,3)15-7-9-19-17(13-15)27-23(29-19)21-11-12-22(31-21)24-28-18-14-16(26(4,5)6)8-10-20(18)30-24/h7-14H,1-6H3
• InChIKey: AIXZBGVLNVRQSS-UHFFFAOYSA-N
• SMILES: CC(C)(C)C1=CC2=C(C=C1)OC(=N2)C3=CC=C(S3)C4=NC5=C(O4)C=CC(=C5)C(C)(C)C

2,5-Bis(5-tert-butylbenzooxazol-2-yl)thiophene(CAT: R022929) is a conjugated heteroaromatic compound designed for advanced materials research. Featuring a central thiophene ring flanked by two benzooxazole units with tert-butyl substitutions, this molecule exhibits strong electron-donating and light-emitting properties. It is widely used in the development of organic semiconductors, OLEDs, and photovoltaic materials due to its extended π-conjugation and thermal stability. The tert-butyl groups enhance solubility and reduce aggregation, making it suitable for solution processing. Its structure supports efficient charge transport and emission characteristics, making it an important building block in the fabrication of optoelectronic devices and functional organic materials.