51980-60-0

Basic information

• Product Name: 4-(2-METHOXY-ETHOXY)-PHENOL
• Synonyms: 4-(2-METHOXY-ETHOXY)-PHENOL;Phenol, 4-(2-Methoxyethoxy)-
• CAS NO: 51980-60-0
• Molecular Formula: C₉H₁₂O₃
• Molecular Weight: 168.19
• Mol File: 51980-60-0.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 4-(2-METHOXY-ETHOXY)-PHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-METHOXY-ETHOXY)-PHENOL(51980-60-0)
• EPA Substance Registry System: 4-(2-METHOXY-ETHOXY)-PHENOL(51980-60-0)

Safety Data

• Statements: 41
• Safety Statements: 26-39
• Hazardous Substances Data: 51980-60-0(Hazardous Substances Data)

Usage

Uses

4-(2-Methoxyethoxy)phenol is a reactant used in the preparation of (2-?fluoro-?4-?methanesulfonylphenyl)?-?{6-?[4-?(3-?isopropyl-?[1,?2,?4]?oxadiazol-?5-?yl)?-?piperidin-?1-?yl]?-?5-?nitro-?pyrimidin-?4-?yl}?-?amine, an oral agonist of orphan G-protein coupled receptor 119.

Upstream product

• 17178-10-8 2-methoxy-ethyl p-toluenesulfonyloxy ester 
• 123-31-9 hydroquinone 
• 623-05-2 (4-hydroxyphenyl)methanol 
• 6482-24-2 2-Bromoethyl methyl ether 
• 109-86-4 2-methoxy-ethanol 

Downstream Products

• 266682-86-4 C₉H₁₁Cl₂O₄P 
• 1439936-20-5 2-bromo-1-{4-(4-(2-methoxyethoxy)phenoxy)-2,6-dimethylphenyl}ethanone 
• 1439936-21-6 4-{4-(4-(2-methoxyethoxy)phenoxy)-2,6-dimethylphenyl}thiazol-2-amine 
• 1439936-18-1 N-(4-{4-(4-(2-methoxyethoxy)phenoxy)-2,6-dimethylphenyl}thiazol-2-yl)isonicotinamide 
• 1439936-44-3 2-fluoro-N-(4-{4-(4-(2-methoxyethoxy)phenoxy)-2,6-dimethylphenyl}thiazol-2-yl)isonicotinamide 
• 1439936-19-2 1-{4-(4-(2-methoxyethoxy)phenoxy)-2,6-dimethylphenyl}ethanone 
• 39255-23-7 1-Bromo-4-(2-Methoxyethoxy)-benzene 
• 1237534-54-1 2,5-bis[4-(2-methoxyethoxy)phenyloxycarbonyl]styrene 
• 1054579-06-4 C₂₁H₂₆N₄O₇ 
• 266682-90-0 C₁₃H₁₉ClNO₆P 
• 872314-71-1 1-(2-bromo-5-chlorobenzyloxy)-4-(2-methoxyethoxy)benzene 
• 359014-85-0 2-(2-{2-[4-(2-Methoxyethoxy)phenoxy]ethoxy}ethoxy)ethanol 

Relevant articles and documents

Pyridine salt / 1,4-dihydropyridine derivative and preparation method thereof

The present invention discloses a pyridine salt / 1,4-dihydropyridine derivative (NAD / NADH analog) with novel structure. The NAD / NADH analog can substitute natural NAD / NADH to be applied to a biochemical system for redox reactions, and can also be used as an electron carrier for the energy transfer of an enzymatic fuel cell. Further, the NAD / NADH analogs provided by the invention are easy to prepare, isolate and purify, and have a high yield.

Mesogen-jacketed liquid crystalline polymers substituted with oligo(oxyethylene) as peripheral chain

Mesogen-jacketed liquid crystalline polymer (MJLCP) is a typical rod-shaped macromolecule. Its unique molecular architecture allows one to tune the geometric parameters of the macromolecular rod. Moreover, the rod surface chemistry can be controlled by de

Enhancing the aqueous solubility of d4T-based phosphoramidate prodrugs

A range of polyether para-substituted phosphoramidates were synthesised and found to have substantially elevated aqueous solubilities compared to the underivatised parent prodrug. A 30-fold increase in aqueous solubility could be achieved without a substantial decrease of in vitro activity against HIV-1. Replacement of the aryl (i.e. phenolic) moiety by tyrosine led to a substantial enhancement in aqueous solubility but also to a decrease in antiviral potency. A previously unobserved trend was identified, relating increased aryl substituent steric bulk to decreased antiviral activity. (C) 2000 Elsevier Science Ltd. All rights reserved.