146370-51-6

Basic information

• Product Name: 1-((2-ETHYLHEXYL)OXY)-4-METHOXYBENZENE
• Synonyms: 1-(2-ethylhexoxy)-4-methoxybenzene
• CAS NO: 146370-51-6
• Molecular Formula: C₁₅H₂₄O₂
• Molecular Weight: 236.35
• Product Categories: Ethers;Organic Building Blocks;Oxygen Compounds
• Mol File: 146370-51-6.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 303-304 °C(lit.)
• Flash Point: >230 °F
• Appearance: /
• Density: 0.960 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.000545mmHg at 25°C
• Refractive Index: n20/D 1.4960(lit.)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 1-((2-ETHYLHEXYL)OXY)-4-METHOXYBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-((2-ETHYLHEXYL)OXY)-4-METHOXYBENZENE(146370-51-6)
• EPA Substance Registry System: 1-((2-ETHYLHEXYL)OXY)-4-METHOXYBENZENE(146370-51-6)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 146370-51-6(Hazardous Substances Data)

Usage

Uses

1-[(2-Ethylhexyl)oxy]-4-methoxybenzene [4-(2-Ethylheptyloxy)benzaldehyde] may be used in the preparation of 1,4-bis(bromomethyl)-2-((2′-ethylhexyl)oxy)-5-methoxybenzene and 1,4-dibromo-2-[(2-ethylhexyl)oxy]-5-methoxy-benzene.

General Description

1-[(2-Ethylhexyl)oxy]-4-methoxybenzene is an intermediate for generating conjugated polymers, which are used in polymer solar cells (PSCs) and light emitting diodes (LED).

InChI:InChI=1/C15H24O2/c1-4-6-7-13(5-2)12-17-15-10-8-14(16-3)9-11-15/h8-11,13H,4-7,12H2,1-3H3

Upstream product

• 104-76-7 2-Ethylhexyl alcohol 
• 696-62-8 para-iodoanisole 
• 18908-66-2 3-bromomethylheptane 
• 150-76-5 4-methoxy-phenol 

Downstream Products

• 209625-37-6 α,α′-dibromo-2-methoxy-5-(2-ethylhexyloxy)xylene 
• 245731-57-1 2-Methoxy-5-(2'-ethylhexyloxy)-1,4-bisacethoxymethylbenzene 
• 406951-48-2 C₄₃H₅₂O₂S₂ 
• 262355-68-0 2,5-bis(trimethylsilylethynyl)-1-(2-ethylhexyloxy)-4-methoxybenzene 
• 262355-69-1 2,5-bis(ethynyl)-1-(2-ethylhexyloxy)-4-methoxybenzene 
• 224558-94-5 1-methoxy-4-(2-ethylhexyloxy)benzene-2,5-diboronic acid 
• 213749-91-8 1,4-bis(cyanomethyl)-2-methoxy-5-(2'-ethylhexyloxy)benzene 
• 245731-58-2 [2-(2'-ethylhexyloxy)-4-(hydroxymethyl)-5-methoxyphenyl]methan-1-ol 
• 203251-22-3 5-(2'-ethylhexyloxy)-2-methoxybenzene-1,4-dicarbaldehyde 
• 181307-48-2 tetraethyl 2-((2-ethylhexyl)oxy)-5-methoxy-1,4-phenylenebis(methylene)bis(phosphonate) 
• 224558-17-2 2-(2-ethylhexyloxy)-5-methoxybenzene-1,4-dibromobenzene 
• 146370-52-7 α,α'-dichloro-p-<5-((2'-ethylhexyl)oxy)-2-methoxy>xylene 

Relevant articles and documents

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

Chain-length dependent nematic ordering of conjugated polymers in a liquid crystal solvent

In this communication we demonstrate the dependence of the solute order parameter on the solute molecular weight for polymer solutes dissolved in liquid crystalline solvents. Using ensemble absorption polarization spectroscopy together with single molecul

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 properties of poly(p-phenylene vinylene) derivatives with hyperbranched structure and containing a nitro substituent

In order to improve efficiency, processability, and stability, two groups of novel poly(p-phenylene vinylene) (PPV) derivatives (P1-P 3 and P4-P6) with hyperbranched structure and containing a nitro substituent were synthesized via a Gilch reaction in different monomer ratios. The properties of the polymers were investigated by using UV-Vis absorption, fluorescence spectroscopy, cyclic voltammetry, and thermogravimetric analysis. The result shows that the band gaps of the PPV derivatives with a nitro substituent were decreased and the polymers had higher molecular weights (106), excellent solubility in common organic solvents, good film-forming ability, and better thermal stability. The polymers can be used as an efficient acceptor material in polymeric solar cells. Graphical abstract: [Figure not available: see fulltext.]