64434-53-3

Upstream product

• 64-17-5 ethanol 
• 71-41-0 pentan-1-ol 
• 66291-82-5 (Z)-1,1,4,4-tetrakis(4-chlorophenyl)-2,3-dichloro-2-butene 
• 141-52-6 sodium ethanolate 
• 5835-98-3 1,1-bis(4-chlorophenyl)-2-propyn-1-ol 
• 90-98-2 4,4'-Dichlorobenzophenone 
• 28437-52-7 1,1'-(3-methoxyprop-1-yne-3,3-diyl)bis(4-chlorobenzene) 
• 1626481-30-8 1,1,4,4-tetrakis(4-chlorophenyl)-4-methoxybut-2-yn-1-ol 

Downstream Products

• 118091-35-3 2-[2,2-Bis-(4-chloro-phenyl)-vinyl]-6-chloro-3-(4-chloro-phenyl)-benzo[b]thiophene 
• 57710-75-5 1,1,4,4-Tetrakis(4-chlorophenyl)-1,3-butadiene 
• 118091-29-5 3,4,6,7-Tetrakis-[bis-(4-chloro-phenyl)-methylene]-[1,2,5]triselenepane 
• 118091-26-2 6,7-Bis-[bis-(4-chloro-phenyl)-methylene]-[1,2,3,4,5]pentathiepane 
• 118091-32-0 2-[2,2-Bis-(4-chloro-phenyl)-vinyl]-6-chloro-3-(4-chloro-phenyl)-benzo[b]selenophene 

Relevant academic research and scientific papers

A Four-Step Synthesis of Substituted 5,11-Dicyano-6,12-diaryltetracenes with Enhanced Stability and High Fluorescence Emission

A four-step synthesis of substituted 5,11-dicyano-6,12-diaryltetracenes was developed, starting from readily available para-substituted benzophenones. The key step of this straightforward route is the complex cascade reaction between tetraaryl[3]cumulenes

Synthesis of cyano-substituted diaryltetracenes from tetraaryl[3]cumulenes

A versatile, two-step synthesis of highly substituted, cyano-functionalized diaryltetracenes has been developed, starting from easily accessible tetraaryl[3]cumulenes. This unprecedented transformation is initiated by [2+2] cycloaddition of tetracyanoethy