146370-51-6

• 

• Basic information

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

• Chemical Properties

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

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany: 3
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 146370-51-6(Hazardous Substances Data)

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146370-51-6 Usage

Description

1-((2-Ethylhexyl)Oxy)-4-Methoxybenzene is an organic compound that serves as an intermediate in the synthesis of various chemical compounds and materials. It is characterized by its ethylhexyloxy and methoxybenzene groups, which contribute to its chemical properties and potential applications.

Uses

1. Used in Chemical Synthesis:
1-((2-Ethylhexyl)Oxy)-4-Methoxybenzene is used as a chemical intermediate for the preparation of 1,4-bis(bromomethyl)-2-((2′-ethylhexyl)oxy)-5-methoxybenzene and 1,4-dibromo-2-[(2-ethylhexyl)oxy]-5-methoxy-benzene. These compounds can be further utilized in the development of advanced materials and products.
2. Used in Polymer Solar Cells (PSCs):
1-((2-Ethylhexyl)Oxy)-4-Methoxybenzene is used as an intermediate for generating conjugated polymers, which are essential components in the fabrication of polymer solar cells. These polymers play a crucial role in the light absorption and charge transport processes within the solar cells, contributing to their overall efficiency and performance.
3. Used in Light Emitting Diodes (LEDs):
In addition to its application in polymer solar cells, 1-((2-Ethylhexyl)Oxy)-4-Methoxybenzene is also utilized in the production of conjugated polymers for light emitting diodes. These polymers are responsible for the emission of light when an electric current is applied, making them vital for the functioning of LEDs in various applications, such as displays, lighting, and signaling devices.

Check Digit Verification of cas no

The CAS Registry Mumber 146370-51-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,3,7 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 146370-51:
(8*1)+(7*4)+(6*6)+(5*3)+(4*7)+(3*0)+(2*5)+(1*1)=126
126 % 10 = 6
So 146370-51-6 is a valid CAS Registry Number.

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

146370-51-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	1-(2-ethylhexoxy)-4-methoxybenzene

1.2 Other means of identification

Product number	-
Other names	1-((2-Ethylhexyl)oxy)-4-methoxybenzene

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:146370-51-6 SDS

146370-51-6Upstream product

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

146370-51-6Downstream Products

• 181307-48-2 tetraethyl 2-((2-ethylhexyl)oxy)-5-methoxy-1,4-phenylenebis(methylene)bis(phosphonate) 
• 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 
• 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 
• 209625-37-6 α,α′-dibromo-2-methoxy-5-(2-ethylhexyloxy)xylene 
• 146370-52-7 α,α'-dichloro-p-<5-((2'-ethylhexyl)oxy)-2-methoxy>xylene 
• 245731-57-1 2-Methoxy-5-(2'-ethylhexyloxy)-1,4-bisacethoxymethylbenzene 
• 224558-94-5 1-methoxy-4-(2-ethylhexyloxy)benzene-2,5-diboronic acid 
• 224558-17-2 2-(2-ethylhexyloxy)-5-methoxybenzene-1,4-dibromobenzene 

146370-51-6Relevant articles and documents

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

Han, Yoon Soo,Kwon, Younghwan,Park, Lee Soon

, p. 141/[421]-153/[433] (2006)

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

Tcherniak, Alexei,Solis Jr., David,Khatua, Saumyakanti,Tangonan, Andrew A.,Lee, T. Randall,Link, Stephan

, p. 12262 - 12263 (2008)

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

Anderson, Nichole,Bagge, Whitney,Webber, Cindy,Zarras, Peter,Davis, Matthew C.

, p. 3903 - 3908 (2008)

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

Li, Ruyu,Mo, Yanjiao,Shi, Rong,Li, Peng,Li, Chengyu,Wang, Zhenjiang,Wang, Xun,Li, Shengbiao

, p. 85 - 90 (2014/03/21)

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.]

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