363622-80-4

Upstream product

• 1154425-90-7 C₂₄H₁₅F₆I 
• 68-12-2 N,N-dimethyl-formamide 
• 363622-51-9 3,5-bis(bromomethyl)benzaldehyde 
• 205578-74-1 tetraethyl [5-(dimethoxymethyl)-1,3-phenylene]bis(methylenephosphonate) 
• 296795-92-1 Tetraethyl 5-formyl-1,3-phenylenebis(methylenephosphonate) 
• 200809-09-2 1,3-bis(bromomethyl)-5-hydroxymethylbenzene 
• 2672-58-4 1,3,5-tris-(methoxycarbonyl)benzene 
• 4464-18-0 1,3,5-tris(hydroxymethyl)benzene 

Downstream Products

• 1154425-95-2 (E,E,E,E,E,E)-4,6-bis[3,5-bis(4-trifluoromethylstyryl)styryl]pyrimidine 

Relevant academic research and scientific papers

V-shaped 4,6-bis(arylvinyl)pyrimidine oligomers: Synthesis and optical properties

(Chemical Equation Presented) A series of V-shaped 4,6-bis(arylvinyl) pyrimidines have been efficiently prepared by aldol condensation between 4,6-dimethylpyrimidine and the appropriate aromatic aldehyde. The methodology also proved successful when dendri

Synthesis, characterization, and optical response of dipolar and non-dipolar poly(phenylenevinylene) dendrimers

New dipolar and non-dipolar poly(phenylenevinylene) dendrimers bearing electron-donating and electron-withdrawing groups have been efficiently synthesized using Heck and Horner-Wadsworth-Emmons reactions. The photoluminescence of these systems may be tuned in the blue zone by choosing the appropriate peripheral groups. Despite the meta-substitution pattern, large Stokes shifts can be observed when π-donor and π-acceptor groups are connected by a m-phenylenevinylene system.