1350699-16-9

Upstream product

• 250726-93-3 2-(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)-4,4,5,5-tetramethyl-2-thiophen-2-yl-1,3,2-dioxaborolane 
• 300806-18-2 5?(4?nitrophenyl)?2,3?dihydrothieno[3,4?b][1,4]dioxine 
• 126213-50-1 3,4-(ethylenedioxy)thiophene 
• 1350699-13-6 1-(5-iodo-3,4-ethylenedioxythien-2-yl)-4-nitrobenzene 
• 193978-23-3 2-thiopheneboronic acid pinacol ester 
• 586-78-7 para-nitrophenyl bromide 

Downstream Products

• 1350699-20-5 2-(4-aminophenyl)-3,4-ethylenedioxy-5,2'-bithiophene 

Relevant academic research and scientific papers

ORGANIC COMPOUNDS, PROCESS FOR PREPARING SAME AND USES IN ELECTRONICS

The present disclosure relates to novel organic compounds, to the processes for preparing same and to the uses thereof, firstly in the electronics field, in particular in the fields referred to as plastic electronics and molecular electronics, and, secondly, in the coatings field, in particular in the fields of adhesion primers and intelligent coatings. The disclosure also relates to a material comprising a novel compound according to the invention.

Synthesis of nitro- and amino-functionalized π-conjugated oligomers incorporating 3,4-ethylenedioxythiophene (EDOT) units

Dissymmetric π-conjugated oligomers incorporating 3,4- ethylenedioxythiophene (EDOT) units and bearing nitro and amino end-groups were synthesized in good yields through Pd-catalyzed Suzuki coupling reactions and direct C-H bond arylation. Their spectrosc