6128-15-0

Upstream product

• 6622-80-6 1,2-Bis(4-iodophenyl)ethane 
• 19829-56-2 4,4'-dibromobibenzyl 

Downstream Products

• 15864-99-0 4,4'-[3,3'-(4,4'-ethane-1,2-diyl-diphenyl)-di-prop-2-ynyl]-bis-morpholine 
• 15865-01-7 C₄₄H₆₀N₂ 
• 1566-58-1 1,2-Bis-(4-<(1-hydroxy-cyclohexyl)-ethyl>-phenyl)-ethan 
• 1566-57-0 1,2-Bis-<4-(3-hydroxy-3-methyl-pentyl)-phenyl>-ethan 
• 1566-59-2 1,2-Bis-<4-(3-hydroxy-3-methyl-butyl)-phenyl>-ethan 
• 1566-49-0 1,2-Bis-<4-(3-hydroxy-3-methyl-pent-1-inyl)-phenyl>-aethan 
• 1566-50-3 1,2-Bis-<4-(3-hydroxy-3-methyl-but-1-inyl)-phenyl>-aethan 
• 15865-05-1 2-[(3-{4-[2-(4-{3-[Bis-(2-hydroxy-ethyl)-amino]-prop-1-ynyl}-phenyl)-ethyl]-phenyl}-prop-2-ynyl)-(2-hydroxy-ethyl)-amino]-ethanol 
• 15865-03-9 [3-(4-{2-[4-(3-Diethylamino-prop-1-ynyl)-phenyl]-ethyl}-phenyl)-prop-2-ynyl]-diethyl-amine 
• 1767-69-7 1,2-Bis-<4-<(1-hydroxy-cyclohexyl)-aethinyl>-phenyl>-aethan 

Relevant academic research and scientific papers

Synthesis of 1,2-biphenylethane based single-molecule diodes

We have described the synthesis of novel biphenylethane-based wires for molecular electronics. Exceptional single-molecule diode behavior was predicted for unsymmetrically substituted biphenylethane derivatives, synthesized here using the so far unexplored unsymmetrically substituted 1,2-bis(4-bromophenyl)ethanes as key intermediates, which were obtained from the corresponding tolane precursor by selective hydrogenation.