1333332-91-4

Upstream product

• 188290-36-0 thiophene 
• 118132-04-0 1,2-Dibromo-4,5-bis(octyloxy)benzene 
• 2563-26-0 4,5-dibromobenzene-1,2-diol 
• 120-80-9 benzene-1,2-diol 
• 111-83-1 1-bromo-octane 
• 54663-78-4 tributyl(thien-2-yl)stannane 
• 4956-41-6 1,2-dioctyloxybenzene 

Downstream Products

• 1333332-94-7 ((5,6-bis(octyloxy)naphtho[1,2-b:4,3-b']dithiophene-2-yl)methyl)triphenylphosphonium bromide 
• 1480585-48-5 C₄₂H₆₈O₂S₂Sn 
• 1480585-18-9 5,5′-(4,5-bis(octyloxy)-1,2-phenylene)bis(2-carbaldehydethiophene) 
• 1480585-16-7 (5,5′-(4,5-bis(octyloxy)-1,2-phenylene)bis(thiophene-5,2 diyl))bis(trimethylsilane) 
• 1480585-13-4 5,5′-(4,5-bis(octyloxy)-1,2-phenylene)bis(2-methylthiophene) 
• 1480585-36-1 5,5′-(4,5-bis(octyloxy)-1,2-phenylene)bis(2-(4,5-bis-(octyloxy)-2-(thiophene-2-yl)phenyl)thiophene) 
• 1480585-10-1 5,5′-(4,5-bis(octyloxy)-1,2-phenylene)bis(2-bromothiophene) 

Relevant academic research and scientific papers

Efficient synthesis of benzo fused tetrathia[7]helicenes

An efficient route toward the synthesis of symmetrical and unsymmetrical benzo fused tetrathia[7]helicenes substituted with electron donor (ED) and electron acceptor (EA) groups is reported. A common, readily available precursor 1,2- bis-(2-thienyl)benzen

Synthesis and optoelectronic property manipulation of conjugated polymer photovoltaic materials based on benzo[d]-dithieno[3,2-b;2′,3′-f]azepine

To develop new conjugated polymers (CPs) based on heteroepines, a soluble azepine moiety of benzo [d]-dithieno [3,2-b; 2′,3′-f]azepine was copolymerized with different building blocks to obtain a series of CPs. A broad absorption range of 300–850 nm and t