252188-95-7

Upstream product

• 18226-42-1 1,3,5-Tris(bromomethyl)benzene 
• 64-19-7 acetic acid 
• 2672-58-4 1,3,5-tris-(methoxycarbonyl)benzene 
• 4464-18-0 1,3,5-tris(hydroxymethyl)benzene 
• 127-09-3 sodium acetate 

Downstream Products

• 1190271-62-5 C₈₇H₁₁₆N₁₈O₂₁S₂ 
• 363622-86-0 [3,5-Bis-((E)-2-{3,5-bis-[(E)-2-(4-methoxy-phenyl)-vinyl]-phenyl}-vinyl)-benzyl]-phosphonic acid diethyl ester 
• 363622-61-1 3,5-bis(p-dodecyloxystyryl)benzyl alcohol 
• 363622-70-2 {3,5-Bis-[(E)-2-(4-cyano-phenyl)-vinyl]-benzyl}-phosphonic acid diethyl ester 
• 363622-68-8 3,5-bis(p-cyanostyryl)-1-bromomethylbenzene 
• 363622-79-1 C₆H₃(C₈H₆CN)2CHO 
• 363622-78-0 3,5-Bis-[(E)-2-(4-dodecyloxy-phenyl)-vinyl]-benzaldehyde 
• 363622-83-7 3,5-Bis-((E)-2-{3,5-bis-[(E)-2-(4-methoxy-phenyl)-vinyl]-phenyl}-vinyl)-benzaldehyde 
• 363622-81-5 [3,5-Bis-((E)-2-{3,5-bis-[(E)-2-(4-methoxy-phenyl)-vinyl]-phenyl}-vinyl)-phenyl]-methanol 
• 363622-69-9 {3,5-Bis-[(E)-2-(4-methoxy-phenyl)-vinyl]-benzyl}-phosphonic acid diethyl ester 
• 363622-63-3 C₆H₃(C₈H₆NC)2CH₂OH 
• 363622-67-7 3,5-bis(p-methoxystyryl)-1-bromomethylbenzene 
• 363622-60-0 {3,5-Bis-[(E)-2-(4-methoxy-phenyl)-vinyl]-phenyl}-methanol 
• 363622-77-9 3,5-Bis-[(E)-2-(4-methoxy-phenyl)-vinyl]-benzaldehyde 

Relevant academic research and scientific papers

A Horner-Wadsworth-Emmons approach to dipolar and non-dipolar poly(phenylenevinylene)dendrimers

The synthesis of first generation phenylenevinylene dendrimers is described. The Horner-Wadsworth-Emmons reaction is used for this purpose. The reported methodology permits the preparation of dipolar and non-dipolar structures. A second generation dendron bearing peripheral electron donor groups is also reported.

Synthesis of novel peptide linkers: Simultaneous cyclization and labeling

Synthesis of novel peptide linkers was accomplished by monocarboxylatlon of 1,3,5-tris(bomomethyl)benzene with a wide variety of carboxylic acids In the presence of diisopropylethylamine. These reagents can be used to simultaneously cyclize and label pept

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.