255901-50-9

Usage

Uses

Used in Organic Material Synthesis:
3,4-(2',2'-dimethylpropylene)dioxithioph is used as a key component in the synthesis of various organic materials, including polymers and conducting materials, due to its unique chemical properties and structural characteristics.
Used in Electronic Device Production:
3 4-(2' 2'-DIMETHYLPROPYLENE)DIOXYTHIOPH is employed in the production of electronic devices and sensors, leveraging its high thermal stability and electrical conductivity to enhance the performance and reliability of these devices.
Used in Sensor Manufacturing:
3,4-(2',2'-dimethylpropylene)dioxithioph is used as a critical material in sensor manufacturing, where its electrical conductivity and thermal stability contribute to the development of innovative and efficient sensing technologies.
Used in Conducting Material Development:
In the development of conducting materials, 3,4-(2',2'-dimethylpropylene)dioxithioph serves as an essential ingredient, providing the necessary electrical conductivity and thermal properties required for advanced applications in various industries.

InChI:InChI=1/C9H12O2S/c1-9(2)5-10-7-3-12-4-8(7)11-6-9/h3-4H,5-6H2,1-2H3

Upstream product

• 51792-34-8 2,3-dimethoxythiophene 
• 126-30-7 2,2-Dimethyl-1,3-propanediol 

Relevant academic research and scientific papers

Indole derivative-proEDOT compound as well as preparation and application thereof

The invention relates to an indole derivative-proEDOT compound as well as preparation and application thereof. The indole derivative is taken as a central core of the compound, a compound 3, 4-(2, 2-dimethyl propylene dioxy) thiophene (proEDOT) is taken as a support arm, and the structure of the compound is shown as a formula (1). The indole derivative-proEDOT compound has the beneficial effects that (1), the Y-shaped material capable of easily forming the net structure is provided, a film is formed through electrochemical polymerization, the obtained film is uniform and shows a large specificsurface area, and good electrochromism and other electrochemical properties are shown; and (2), a film prepared by taking the compound as a monomer through electrochemistry can be randomly switched from yellow to green (0.9 V) and to gray (1.2 V), the optical contrast ratio is 20%-40%, the response time is 0.5-4s, and the compound shows relatively good spectral electrochemical stability in any waveband and has a good application prospect.

Solid electrolyte and Solid electrolyte capacitor including the same

In the present invention, disclosed are a solid electrolyte consisting of conductive polymers polymerized by a novel thiophene derivative, and a solid electrolyte condenser including the same wherein the thiophene derivative denoted by chemical formula 3 can be used for forming the conductive polymer-made solid electrolyte where X and Y are independently oxygen (O) atom, sulfur (S) atom or selenium (Se) atom, and n and m are independently integers between 0 and 4 and are different numbers in chemical formula 3.COPYRIGHT KIPO 2015

Triphenylamine-based dyes bearing functionalized 3,4- propylenedioxythiophene linkers with enhanced performance for dye-sensitized solar cells

Chemical Equation Presented Introduction of modified 3,4-propylenedioxythiophene units into triphenylamine-based dyes is found to enhance light capturing, suppress dye aggregation, and remarkably retard charge recombination in dye-sensitized solar cells. Open circuit voltages of the as-synthesized dyes (～800 mV) are much higher than that with a thiophene congener (720 mV) under similar conditions as a result of self-passivation benefiting from their three-dimensional branched structures.