Switching of the π-electronic conjugations in the reduction of a dithienylethene-fused p-benzoquinone was written by Saito, Eiji;Ako, Takumi;Kobori, Yasuhiro;Tsuda, Akihiko. And the article was included in RSC Advances in 2017.Application In Synthesis of 2,5-Dimethylthiophene The following contents are mentioned in the article:
The electron accepting character of a dithienylethene-fused p-benzoquinone derivative is significantly reduced upon ring-closing isomerization. Visible light unlocks the π-electronic conjugation of the quinone so it can be utilized for a light-driven oxidation reaction. This study involved multiple reactions and reactants, such as 2,5-Dimethylthiophene (cas: 638-02-8Application In Synthesis of 2,5-Dimethylthiophene).
2,5-Dimethylthiophene (cas: 638-02-8) belongs to benzothiophene derivatives. Benzothiophene is relatively a stable molecule. The core structure is a part of various pharmaceutical substances and natural products. It is found within the chemical structures of pharmaceutical drugs such as zileuton, raloxifene, and sertaconazole, and also BTCP.Application In Synthesis of 2,5-Dimethylthiophene
Referemce:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem