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| Product | Description | |
|---|---|---|
| 3,4-Dimethoxythiophene | 3,4-Dimethoxythiophene (DMOT) is a monomer and a precursor which can be synthesized by ring closure reaction of 2,3-dimethoxy-1,3-butadiene and sulfur dichloride in hexane medium. It is an oligothiphene that is majorly used in the development of electroactive materials for organic electronics based applications. Uses: Building block in the synthesis of an n2s2-n4 porphyrin dyad used to study photoinduced energy transfer. dmot can be trans-esterified to form 3,4-ethylenendioxythiophene (edot). it can further be polymerized to produce pedot which can be used as a conductive polymer in π-conjugated systems. it can be polymerized to form poly(dimethoxythiphenes) which can potentially be used in the fabrication energy storage devices on electrochemical doping. Group: other electronic materials synthetic tools and reagents. Alternative Names: Thiophene, 3,4-Dimethoxy-. CAS No. 51792-34-8. Pack Sizes: Packaging 5 g in glass bottle. Product ID: 3,4-dimethoxythiophene. Molecular formula: 144.19. Mole weight: C6H8O2S. COc1cscc1OC. 1S/C6H8O2S/c1-7-5-3-9-4-6 (5)8-2/h3-4H, 1-2H3. ZUDCKLVMBAXBIF-UHFFFAOYSA-N. ≥ 97%. |  |
| 3,4-Dimethoxythiophene | 97%. Group: Synthetic tools and reagents. |  |
| 3,4-Dimethoxythiophene, 97% | 3,4-Dimethoxythiophene, 97%. Group: Synthetic tools and reagents. CAS No. 51792-34-8. Product ID: 3,4-dimethoxythiophene. Molecular formula: 144.19g/mol. Mole weight: C6H8O2S. COC1=CSC=C1OC. InChI=1S/C6H8O2S/c1-7-5-3-9-4-6 (5)8-2/h3-4H, 1-2H3. ZUDCKLVMBAXBIF-UHFFFAOYSA-N. | |
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