714201-40-8

Upstream product

• 98437-23-1 benzo[b]thiophene-2-boronic acid 
• 95-15-8 Benzo[b]thiophene 
• 5344-78-5 4-bromo-3-nitroanizole 
• 397882-60-9 2-(2'-nitro-4'-methoxyphenyl)benzo[b]thiophene 

Downstream Products

• 950852-00-3 3-methoxy-6-phenylbenzothieno[3,2-c]quinoline 
• 876731-43-0 3-methoxy-6-(m-methoxyphenyl)benzothieno[3,2-c]quinoline 
• 714201-41-9 N-(2-benzo[b]thiophen-2-yl-5-methoxy-phenyl)-acetamide 

Relevant academic research and scientific papers

Synthesis of fluorescent rhodamine dyes using an extension of the Heck reaction

Both benzo[b]thiophene and indole containing rhodamine dyes were synthesized according to a new pathway requiring a Heck-type coupling and a Pictet-Spengler reaction. The electron-rich indolic dye was shown to have noteworthy absorption and emission maxim

Heck-like coupling and Pictet-Spengler reaction for the synthesis of benzothieno[3,2-c]quinolines

A series of 6-arylbenzothieno[3,2-c]quinolines were synthesised in three steps from benzo[b]thiophene. After a selective Heck-type coupling of benzo[b]thiophene with different o-nitroaryl bromides to obtain 2-(o-nitroaryl)benzo[b]thiophenes, corresponding

Rational design and synthesis of a novel class of highly fluorescent rhodamine dyes that have strong absorption at long wavelengths

A novel class of strongly fluorescent rhodamine dyes were designed and synthesized by extending the π conjugation of chromophore with limited flexibility. These dyes were shown to have longer absorption in the range of 581 to 631 nm with quantum yields between 0.64 and 0.89.