1496785-69-3

Upstream product

• 78531-62-1 8-([1,1'-biphenyl]-4-yl)-1,4-dioxaspiro[4.5]decan-8-ol 
• 4746-97-8 cyclohexanedione monoethylene ketal 

Downstream Products

• 1609571-97-2 C₄₁H₄₂O₅ 
• 1609571-98-3 C₄₁H₃₉NO₄ 
• 1609571-99-4 C₄₀H₃₉ClO₄ 
• 1609571-93-8 1-(4-bromophenyl)-4-(biphenyl-4-yl)-4-(methoxymethyloxy)cyclohexanol 
• 1609572-02-2 C₃₇H₂₈O 
• 1080024-69-6 C₃₇H₂₅N 
• 1609572-03-3 C₃₆H₂₅Cl 
• 1609571-95-0 1-(4-bromophenyl)-4-(biphenyl-4-yl)-1,4-bis(methoxymethyloxy)cyclohexane 
• 1609571-91-6 4-(biphenyl-4-yl)-4-(methoxymethyloxy)cyclohexanone 

Relevant academic research and scientific papers

Making nonsymmetrical bricks: Synthesis of insoluble dipolar sexiphenyls

A versatile synthesis of nonsymmetrical, terminally substituted p-sexiphenyl (6P) derivatives has been developed. The synthesis makes use of a nonsymmetrical starting material as well as modular functionalization using Suzuki cross-coupling to yield a soluble precursor, which finally is converted to the insoluble target 6P derivatives. These derivatives display similar electronic and optical properties to the parent 6P, yet the permanent dipole along their molecular axis allows for tuning of their self-assembly on various substrate surfaces.