64806-63-9

Basic information

• Product Name: Benzene, (3-phenoxypropyl)-
• Synonyms: 3-phenylpropoxybenzene
• CAS NO: 64806-63-9
• Molecular Formula: C15H16O
• Molecular Weight: 212.291
• Mol File: 64806-63-9.mol
• Article Data: 26

Chemical Properties

• CAS DataBase Reference: Benzene, (3-phenoxypropyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, (3-phenoxypropyl)-(64806-63-9)
• EPA Substance Registry System: Benzene, (3-phenoxypropyl)-(64806-63-9)

Safety Data

• Hazardous Substances Data: 64806-63-9(Hazardous Substances Data)

Upstream product

• 37464-41-8 phenyl 3-phenyl-allyl ether 
• 122-97-4 3-Phenyl-1-propanol 
• 589-10-6 phenoxyethyl bromide 
• 139-02-6 sodium phenoxide 
• 104-52-9 phenylpropyl chloride 
• 90535-47-0 (3-phenoxypropyl)boronic acid 
• 71-43-2 benzene 
• 726-26-1 phenyl 3-phenylpropanoate 
• 501-52-0 3-Phenylpropionic acid 
• 1746-13-0 allyl phenyl ether 
• 98-80-6 phenylboronic acid 
• 6921-34-2 benzylmagnesium chloride 
• 4119-41-9 1-iodo-3-phenylpropan 
• 1821-12-1 4-Phenylbutyric acid 

Downstream Products

• 637-59-2 1-Bromo-3-phenylpropane 
• 15185-05-4 4-phenylcoumarin 
• 14794-60-6 N-Hydroxy-2-[4-(3-phenyl-propoxy)-phenyl]-acetamide 
• 15560-84-6 [4-(3-Phenyl-propoxy)-phenyl]-acetic acid ethyl ester 

Relevant articles and documents

Structure and reactivity in neutral organic electron donors derived from 4-dimethylaminopyridine

The effects on the redox properties of modifying the molecular skeleton of neutral bis-2-(4-dimethylamino)pyridinylidene electron donors, derived from 4-dimethylaminopyridine (4-DMAP), have been explored, by varying two parameters: (i) the length of a polymethylene chain linking the two pyridine-derived rings and (ii) the nature of the nitrogen substituents on the 4 and 4″ positions of the precursor pyridines. Restricting the bridge length to two methylene units significantly altered the redox profile, while changes in the nitrogen-substituents at the 4 and 4' positions led to only slight changes in the redox potentials.

Base-Mediated O-Arylation of Alcohols and Phenols by Triarylsulfonium Triflates

A mild and efficient protocol for O-arylation of alcohols and phenols (ROH) by triarylsulfonium triflates was developed under transition-metal-free conditions. Various alcohols, including primary, secondary and tertiary, and phenols bearing either electron-donating or electron-withdrawing groups on the aryl rings were smoothly converted to form the corresponding aromatic ethers in moderate to excellent yields. The reactions were conducted at 50 or 80 °C for 24 h in the presence of a certain base and showed good functional group tolerance. The base-mediated arylation with asymmetric triarylsulfonium salts could selectively transfer the aryl groups of sulfoniums to ROH, depending on their inherent electronic nature. The mechanistic studies revealed that the reaction might proceed through the nucleophilic attack of the in situ formed alkoxy or phenoxy anions at the aromatic carbon atoms of the C?S bonds of triarylsulfonium cations to furnish the target products.

Metal-Free I2-Catalyzed Highly Selective Dehydrogenative Coupling of Alcohols and Cyclohexenones

The I2 catalyzed highly selective oxidative condensation of cyclohexenones and alcohols for the synthesis of aryl alkyl ethers has been described. DMSO is employed as the mild terminal oxidant. This novel methodology offers a metal-free reaction condition, operational simplicity and broad substrate scope to afford valuable products from inexpensive reagents. Various meta-substituted aromatic ethers which are hardly synthesized from the reported methods requiring meta-substituted phenols, are efficiently prepared by the present protocol.