134366-04-4

Usage

Structure

A pyrrole-2,5-dione derivative containing a trifluorophenyl group

Usage

Commonly used as a building block in the synthesis of pharmaceutical compounds and agrochemicals

Biological activities

Studied for potential antimicrobial and anticancer properties

Importance in research

Unique chemical structure makes it a valuable tool in organic chemistry research and drug discovery

Downstream Products

• 1217683-90-3 N-(2,4,6-trifluorophenyl)-7-[bis(4-bromophenyl)methylidene]bicyclo[2.2.1]hept-2-ene-5,6-dicarboximide 
• 1217657-52-7 N-(2,4,6-trifluorophenyl)-7-[bis(4-fluorophenyl)methylidene]bicyclo[2.2.1]hept-2-ene-5,6-dicarboximide 

Relevant academic research and scientific papers

Copolymers of methyl methacrylate with N-trifluorophenyl maleimides: High glass transition temperature and low birefringence polymers

Copolymers of methyl methacrylate (MMA) with 2,3,4- and 2,4,6-trifluorophenyl maleimides (TFPMIs) were synthesized by a free radical initiator, azobisisobutyronitrile, in 1,4-dioxane and also in bulk. The refractive indexes of the copolymers were in the range of 1.49-1.52 at 532 nm. The Tgs were 133-195 °C depending on copolymer compositions. In addition, the copolymers were thermally stable, Td > 350 °C. The orientational and photoelastic birefringence of the copolymers were also investigated. As both of the orientational and photoelastic birefringences of PMMA are negative, whereas those of poly(TFPMI)s are positive, we could obtain nearly zero orientational and photoelastic birefringence polymers when the ratios of 2,3,4-TFPMI/MMA were 15/85 and 5/95 mol %, respectively. For 2,4,6-TFPMI, zero orientational and photoelastic birefringences could be obtained when the ratios of 2,4,6-TFPMI/MMA were 12/88 and 3/97 mol %, respectively. The Tgs of those copolymers with zero birefringences were in the range of 135-140 °C. Copyright