119967-49-6

Basic information

• Product Name: Ethanol, 2-(3-pyridinyloxy)- (9CI)
• Synonyms: Ethanol, 2-(3-pyridinyloxy)- (9CI);2-(pyridin-3-yloxy)ethanol;2-(3-Pyridyloxy)ethanol;2-(3-Pyridinyloxy)ethanol;2-(Pyridyl-3-yloxy)ethanol;3-(2-hydroxyethoxy)pyridine
• CAS NO: 119967-49-6
• Molecular Formula: C₇H₉NO₂
• Molecular Weight: 139.15186
• Product Categories: PYRIDINE
• Mol File: 119967-49-6.mol
• Article Data: 11

Chemical Properties

• Melting Point: 98-99℃
• Boiling Point: 272℃
• Flash Point: 119℃
• Appearance: colorless or light yellow liquid
• Density: 1.153
• Vapor Pressure: 0.00298mmHg at 25°C
• Refractive Index: 1.528
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Ethanol, 2-(3-pyridinyloxy)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanol, 2-(3-pyridinyloxy)- (9CI)(119967-49-6)
• EPA Substance Registry System: Ethanol, 2-(3-pyridinyloxy)- (9CI)(119967-49-6)

Safety Data

• Hazardous Substances Data: 119967-49-6(Hazardous Substances Data)

Usage

General Description

Ethanol, 2-(3-pyridinyloxy)- (9CI) is a chemical compound with the molecular formula C7H7NO2. It is a derivative of ethanol with a 3-pyridinyloxy group attached to the carbon chain. Ethanol, 2-(3-pyridinyloxy)- (9CI) has various applications in the pharmaceutical and chemical industries, serving as a building block for the synthesis of other organic compounds. It may also be used as a solvent or reagent in laboratory settings. Additionally, it has potential biological activities, making it of interest for research and development in the field of medicine. However, like all chemicals, it should be handled and used with proper precautions and under controlled conditions to ensure safety.

InChI:InChI=1/C7H9NO2/c9-4-5-10-7-2-1-3-8-6-7/h1-3,6,9H,4-5H2

Upstream product

• 75-21-8 oxirane 
• 109-00-2 3-HYDROXYPYRIDINE 
• 626-55-1 3-Bromopyridine 
• 107-21-1 ethylene glycol 
• 107-07-3 2-chloro-ethanol 
• 96-49-1 [1,3]-dioxolan-2-one 

Downstream Products

• 104818-90-8 3-vinyloxypyridine 

Relevant articles and documents

THIAZOLIDINONE COMPOUNDS AND USE THEREOF

A pharmaceutical composition containing a compound of Formula (I) for treating an opioid receptor-associated condition. Also disclosed is a method for treating an opioid receptor-associated condition using such a compound. Further disclosed are two sets of thiazolidinone compounds of formula (I): (i) compounds each having an enantiomeric excess greater than 90% and (ii) compounds each being substituted with deuterium.

Copper(ii)-catalyzed C-O coupling of aryl bromides with aliphatic diols: Synthesis of ethers, phenols, and benzo-fused cyclic ethers

A highly efficient copper-catalyzed C-O cross-coupling reaction between aryl bromides and aliphatic diols has been developed employing a cheaper, more efficient, and easily removable copper(ii) catalyst. A broad range of aryl bromides were coupled with aliphatic diols of different lengths using 5 mol% CuCl2 and 3 equivalents of K2CO3 in the absence of any other ligands or solvents to afford the corresponding hydroxyalkyl aryl ethers in good to excellent yields. In this newly developed protocol, aliphatic diols have multilateral functions as coupling reactants, ligands, and solvents. The resulting hydroxyalkyl aryl ethers were further readily converted into the corresponding phenols, presenting a valuable alternative way to phenols from aryl bromides. Furthermore, it was demonstrated that they are useful intermediates for more advanced molecules such as benzofurans and benzo-fused cyclic ethers. This journal is

Synthetic access to new pyridone derivatives through the alkylation reactions of hydroxypyridines with epoxides

General methods for the preparation of a variety of pyridone and oxypyridine derivatives are described. 2-,3-,4-Hydroxy pyridine and 2-pyridinemethanol were alkylated with ethylene-, propylene-, and stryrene-oxide and epichlorohydrin in the presence of di