146370-52-7

Usage

Uses

Conducting polymer precursor.

InChI:InChI=1/C17H26Cl2O2/c1-4-6-7-13(5-2)12-21-17-9-14(10-18)16(20-3)8-15(17)11-19/h8-9,13H,4-7,10-12H2,1-3H3

Upstream product

• 18908-66-2 3-bromomethylheptane 
• 150-76-5 4-methoxy-phenol 
• 50-00-0 formaldehyd 
• 146370-51-6 1-((2-ethylhexyl)oxy)-4-methoxybenzene 

Downstream Products

• 213749-91-8 1,4-bis(cyanomethyl)-2-methoxy-5-(2'-ethylhexyloxy)benzene 
• 203251-22-3 5-(2'-ethylhexyloxy)-2-methoxybenzene-1,4-dicarbaldehyde 
• 245731-58-2 [2-(2'-ethylhexyloxy)-4-(hydroxymethyl)-5-methoxyphenyl]methan-1-ol 
• 500206-28-0 2,5-bis-{2-(5'-bromothienyl)-1-cyanovinyl}-1-(2'-ethylhexyloxy)-4-methoxybenzene 
• 181307-48-2 tetraethyl 2-((2-ethylhexyl)oxy)-5-methoxy-1,4-phenylenebis(methylene)bis(phosphonate) 

Relevant academic research and scientific papers

White light emission transparent polymer nanocomposites with novel poly(p-phenylene vinylene) derivatives and surface functionalized CdSe/ZnS NCs

A series of new polymers with conjugated poly(p-phenylene vinylene) units and non-conjugated poly(p-xylylene) units containing vinyl and carboxyl groups were synthesized. The monodisperse CdSe/ZnS nanocrystals with a red light emission were prepared by us

Procedure for the rapid synthesis of the monomer 1,4-bis(chloromethyl)-2- (2-ethylhexyloxy)-5-methoxybenzene

The alkylation of 4-methoxyphenol with 2-ethylhexyl bromide was accelerated by using potassium tert-butoxide in dimethylformamide. Subsequent chloromethylation occurred quickly using acetic acid as a cosolvent to give the poly[(2-(2-ethylhexyloxy)-5-metho

Synthesis and characterization of conjugated copolymers, and their color tuning with molecular microstructure

Poly(2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylene vinylene-co-1,4-phenylene vinylene) (MEH-R) and poly(2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylene vinylene-alt-1,4-phenylene vinylene) (MEH-A50) containing phenylene vinylene (PV) unit and alkoxyphenylene vi

Synthesis, characterization, and electroluminescence of new conjugated polyfluorene derivatives containing various dyes as comonomers

Four new fluorene-based alternating polymers (PFR1-S, PFR2-S, PFR3-S, and PFR4-S) containing different comonomers (R1, R2, R3, and R4) have been designed, synthesized, and characterized. These polymers were found to be thermally stable and readily soluble

Chemical tuning of the electronic properties of poly(p-phenylenevinylene)-based copolymers

Molecular engineering has allowed the control of the HOMO-LUMO gap energy in a family of conjugated polymers based on poly(p-phenylenevinylene) (PPV). Random copolymerization of 1 and 6 afforded precursor polymers 10 with two different leaving groups. Tre