127462-96-8

Upstream product

• 106456-88-6 4-(5,5-dimethyl-1,3-dioxan-2-yl)benzaldehyde 
• 126-30-7 2,2-Dimethyl-1,3-propanediol 
• 623-27-8 terephthalaldehyde, 
• 1571-08-0 methyl 4-formylbenzoate 
• 138536-73-9 4-(5,5-Dimethyl-[1,3]dioxan-2-yl)-benzoic acid methyl ester 

Downstream Products

• 152424-25-4 2-(4-bromomethylphenyl)-5,5-dimethyl[1,3]dioxane 
• 138536-87-5 5-<2,6-bis(benzyloxy)phenyl>-15-(4-formylphenyl)-2,8,12,18-tetrahexyl-3,7,13,17-tetramethylporphine 
• 950608-78-3 5,5-Dimethyl-2-(4-{(E)-2-[4-((E)-2-{4-[(E)-2-(3,4,5-tris-dodecyloxy-phenyl)-vinyl]-phenyl}-vinyl)-phenyl]-vinyl}-phenyl)-[1,3]dioxane 
• 404822-87-3 (4-(5,5-dimethyl-[1,3]-dioxan-2-yl)benzyl)phosphonic aciddiethyl ester 
• 106456-88-6 4-(5,5-dimethyl-1,3-dioxan-2-yl)benzaldehyde 

Relevant academic research and scientific papers

Directional Supramolecular Polymerization in a Dynamic Microsolution: A Linearly Moving Polymer's End Striking Monomers

Although directional chain reactions are common in nature's self-assembly processes and in covalent polymerizations, it has been challenging to perform such processes in artificial one-dimensional self-assembling systems. In this paper, we describe a syst

Functionalization of [60]fullerene with new light-collecting oligophenylenevinylene-terminated dendritic wedges

New oligophenylenevinylene-terminated phenylenevinylene dendrons have been prepared and attached to C60 by a 1,3-dipolar cycloaddition of the azomethine ylides generated in situ from the dendritic aldehydes and N-methylglycine. Preliminary phot

Synthesis and Fluorescence Properties of Selectively Metallated Diporphyrins with Electron-Accepting Moieties

Synthesis of selectively metallated diporphyrins with electron-accepting moieties is described.Steady-state fluorescence spectra of these compounds showed substantial quenching of the fluorescence of the free-base porphyrin.A possible "superexchange" mechanism of long-range electron transfer is discussed.