5-Fluoro-4,7-bis(5-(trimethylstannyl)thiophen-2-yl)benzo[c][1,2,5]thiadiazole

• CAT Number: L018244
• CAS Number: 1611002-56-2
• Molecular Formula: C20H23FN2S3Sn2
• Molecular Weight: 644.04
• Purity: ≥95%
• IUPAC Name: [5-[5-fluoro-4-(5-trimethylstannylthiophen-2-yl)-2,1,3-benzothiadiazol-7-yl]thiophen-2-yl]-trimethylstannane
• InChI: InChI=1S/C14H5FN2S3.6CH3.2Sn/c15-9-7-8(10-3-1-5-18-10)13-14(17-20-16-13)12(9)11-4-2-6-19-11;;;;;;;;/h1-4,7H;6*1H3
• InChIKey: MBFGAZRENCVSAJ-UHFFFAOYSA-N

5-Fluoro-4,7-bis(5-(trimethylstannyl)thiophen-2-yl)benzo[c][1,2,5]thiadiazole(CAT: L018244) is a highly specialized compound often used in materials science and organic electronics, particularly in the development of semiconducting polymers and photovoltaic materials. Its structure combines fluorine-substituted benzo[c][1,2,5]thiadiazole with trimethylstannyl-functionalized thiophene groups, enhancing its electronic properties and enabling precise tuning of the molecule’s optoelectronic characteristics. The trimethylstannyl groups facilitate cross-coupling reactions, such as Stille coupling, allowing for the construction of complex conjugated systems. This compound is ideal for applications in organic solar cells, field-effect transistors, and light-emitting diodes, where its electron-accepting properties contribute to efficient charge transport and energy conversion in advanced material research.