607-58-9

Basic information

• Product Name: 1-Benzyloxynaphthalene
• Synonyms: 1-Benzyloxynaphthalene;Benzyl naphthyl ether;Naphthyl benzyl ether;Benzyl alpha-naphthyl ether;1-(PHENYLMETHOXY)NAPHTHALENE;(1-Naphtyl)benzyl ether;1-Naphtylbenzyl ether;1-Naphthyl Benzyl Ether
• CAS NO: 607-58-9
• Molecular Formula: C₁₇H₁₄O
• Molecular Weight: 234.29246
• Product Categories: Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals
• Mol File: 607-58-9.mol
• Article Data: 25

Chemical Properties

• Melting Point: 73.5-74 °C
• Boiling Point: 388.1°C at 760 mmHg
• Flash Point: 156.4°C
• Appearance: /
• Density: 1.125g/cm³
• Vapor Pressure: 7.02E-06mmHg at 25°C
• Refractive Index: 1.642
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: Chloroform (Slightly), DMSO (Slightly), Ethyl Acetate (Slightly)
• CAS DataBase Reference: 1-Benzyloxynaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Benzyloxynaphthalene(607-58-9)
• EPA Substance Registry System: 1-Benzyloxynaphthalene(607-58-9)

Safety Data

• Hazardous Substances Data: 607-58-9(Hazardous Substances Data)

Usage

Description

1-Benzyloxynaphthalene is a naphthyl ether, a type of organic compound characterized by the presence of an ether functional group (-O-) connecting two aromatic rings. It is known for its unique chemical properties and potential applications in various fields.

Uses

Used in Coal Direct Liquefaction Studies:
1-Benzyloxynaphthalene is used as a research compound for the improvement of coal direct liquefaction by steam pretreatment. Its presence in the process is believed to enhance the efficiency and effectiveness of the liquefaction, leading to better conversion rates and potentially more sustainable energy production methods. This application is particularly relevant in the field of energy and materials science, where the development of cleaner and more efficient energy sources is of utmost importance.

InChI:InChI=1/C17H14O/c1-2-7-14(8-3-1)13-18-17-12-6-10-15-9-4-5-11-16(15)17/h1-12H,13H2

Upstream product

• 90-15-3 α-naphthol 
• 3204-68-0 benzyldimethylphenylammonium chloride 
• 100-44-7 benzyl chloride 
• 86-57-7 1-Nitronaphthalene 
• 100-51-6 benzyl alcohol 
• 53772-44-4 benzyloxydiphenylphosphine 
• 100-39-0 benzyl bromide 
• 124-41-4 sodium methylate 
• 260783-80-0 N,N,N--trimethyl--1--phenylmethanaminium trifluoromethanesulfonate 
• 90-14-2 1-Iodonaphthalene 
• 3433-80-5 1-Bromo-2-bromomethyl-benzene 
• 90-11-9 1-Bromonaphthalene 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 93654-98-9 phenyl acetic acid naphthalen-1-yl ester 

Downstream Products

• 213455-52-8 4-benzyloxynaphthalene-1-carbaldehyde 
• 642-28-4 phenyl(1-naphthyl)methanol 
• 90-15-3 α-naphthol 
• 138865-41-5 1-(benzyloxy)-4-bromonaphthalene 
• 108-88-3 toluene 
• 103-29-7 1,1'-(1,2-ethanediyl)bisbenzene 
• 33490-96-9 1-naphthoxyl radical 
• 92929-51-6 4-nitro-1-naphthyl benzoate 
• 3960-21-2 1,2-di(naphthyl)ethene 
• 135505-52-1 N-(1-Naphthalenyl)-N-phenyl-1-naphthalenemethanamine 
• 28178-96-3 4-(phenylmethyl)-1-naphthalenol 
• 830-81-9 1-naphthyl acetate 
• 20009-25-0 allyl naphthyl ether 

Relevant articles and documents

Pd-Catalyzed Etherification of Nitroarenes

The Pd-catalyzed etherification of nitroarenes with arenols has been achieved using a new rationally designed ligand. Mechanistic insights were used to design the ligand so that both the oxidative addition and reductive elimination steps of a plausible catalytic cycle were facilitated. The catalytic system established here provides direct access to a range of unsymmetrical diaryl ethers from nitroarenes.

Aromatic ether compound or the sulfhydryl compound

[Problem] Aromatic ether compounds and aromatic sulfide compound of this new technology to[Solution] In general formula (1a), (1b), (1c) palladium or nickel compound or a phosphine compound represented by the compound comprising a transition metal compound in the presence of a transition metal catalyst, (A1) is represented by compounds having hydroxy carbon C a-OH or (A2) with a compound represented by the sulfhydryl carbon C a-SH, nitro group (- NO2 ) To react with an aromatic nitro compound (B), (A1) to the compound of the aromatic nitro compound (C1) or the reaction product of an aromatic ether compounds (B) hetero coupling (A2) of the compounds of the reaction product of an aromatic sulfide compound of an aromatic nitro compound (C2) generating (B) hetero coupling characterized by comprising the step of, aromatic ether compounds or aromatic sulfide compound. [Drawing] no

MCM-41-immobilized 1,10-phenanthroline-copper(i) complex: A highly efficient and recyclable catalyst for the coupling of aryl iodides with aliphatic alcohols

A heterogeneous C-O coupling reaction between aryl iodides and aliphatic alcohols was achieved in neat alcohol or toluene at 110 °C in the presence of 10 mol% of the MCM-41-immobilized 1,10-phenanthroline-copper(i) complex [MCM-41-1,10-phen-CuI] with Cs2CO3 as a base, yielding a variety of aryl alkyl ethers in good to excellent yields. The new heterogeneous copper catalyst can easily be prepared by a simple procedure from commercially available and inexpensive reagents, and recovered by filtration of the reaction solution and recycled at least 8 times without significant loss of activity.