91967-71-4

Basic information

• Product Name: (1-propoxyethyl)benzene
• Synonyms: (1-Propoxyethyl)benzene; 1-Phenylethyl propyl ether; benzene, (1-propoxyethyl)-
• CAS NO: 91967-71-4
• Molecular Formula: C₁₁H₁₆O
• Molecular Weight: 164.2441
• Mol File: 91967-71-4.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 204.6°C at 760 mmHg
• Flash Point: 75.5°C
• Density: 0.918g/cm³
• Vapor Pressure: 0.373mmHg at 25°C
• Refractive Index: 1.487
• CAS DataBase Reference: (1-propoxyethyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (1-propoxyethyl)benzene(91967-71-4)
• EPA Substance Registry System: (1-propoxyethyl)benzene(91967-71-4)

Safety Data

• Hazardous Substances Data: 91967-71-4(Hazardous Substances Data)

Upstream product

• 100-42-5 styrene 
• 71-23-8 propan-1-ol 
• 133745-75-2 N-fluorobis(benzenesulfon)imide 
• 98-85-1 1-Phenylethanol 

Downstream Products

• 100-42-5 styrene 
• 71-23-8 propan-1-ol 

Relevant articles and documents

Sulfated tungstate as hydroxyl group activator for preparation of benzyl, including p-methoxybenzyl ethers of alcohols and phenols

Sulfated tungstate was found to be an effective heterogeneous and reusable catalyst for hydroxy group activation–mediated preparation of benzylic ethers including p-methoxybenzylic ethers of a wide range of alcohols and phenols under mild reaction conditions.

Palladium-catalyzed inter- and intramolecular hydroamination of styrenes coupled with alcohol oxidation using N-fluorobenzenesulfonimide as the oxidant

Palladium-catalyzed inter- and intramolecular hydroaminations of styrenes that are coupled to alcohol oxidation under oxidative condition are reported. The fluorination reagent NFSI is used as the nitrogen source as well as the oxidant. Bidental nitrogen

Efficient addition of alcohols, amines and phenol to unactivated alkenes by AuIII or PdII stabilized by CuCl2

The nucleophilic addition of alcohols, amines and phenol to unactivated alkenes catalyzed by cationic gold and palladium becomes limited due to the fast reduction into metallic gold under reaction conditions. The presence of CuCl2 retards the reduction of AuIII and PdII, strongly increasing the turnover number of gold and palladium catalysts. It is shown that new AuIII-CuCl2 and PdII-CuCl 2 catalysts are active and selective for the nucleophilic addition of alcohols, amines and phenol to unactivated alkenes. This journal is The Royal Society of Chemistry.