61982-86-3

Usage

Naphthalene family

1-Methoxy-5-phenylnaphthalene belongs to the naphthalene family, which is a group of organic compounds consisting of two fused benzene rings.

Industrial applications

1-Methoxy-5-phenylnaphthalene is widely used in the pharmaceutical and chemical industries as a building block for synthesizing various organic compounds.

Fluorescence properties

The compound exhibits strong fluorescence, making it useful in the development of fluorescent dyes and markers.

Optoelectronic applications

1-Methoxy-5-phenylnaphthalene has been studied for its potential use in organic light-emitting diodes (OLEDs) and other optoelectronic applications due to its unique optical and electronic properties.

Health and environmental hazards

It is important to handle 1-Methoxy-5-phenylnaphthalene with care, as it may pose health and environmental risks if not used and disposed of properly.

Upstream product

• 229031-55-4 methyl-(5-phenyl-7,8-dihydro-[1]naphthyl)-ether 
• 33892-75-0 5-Methoxy-1-tetralone 
• 33567-59-8 (2-methoxy-phenyl)-acetaldehyde 
• 536-74-3 phenylacetylene 
• 74924-95-1 1-bromo-5-methoxynaphthalene 
• 98-80-6 phenylboronic acid 

Downstream Products

• 61982-94-3 5-phenyl-1-naphthol 

Relevant academic research and scientific papers

Synthesis of naphthalene derivatives through inexpensive BF 3·Et2O-catalyzed annulation reaction of arylacetaldehydes with arylalkynes

An inexpensive BF3·Et2O-catalyzed annulation reaction of arylacetaldehydes with arylalkynes has been developed. Various substituted phenylacetaldehydes and phenylacetylenes can undergo this reaction, producing corresponding α-aryl su

Excited state intramolecular proton transfer (ESIPT) from phenol to carbon in selected phenylnaphthols and naphthylphenols

ESIPT and solvent-assisted ESPT in isomeric phenyl naphthols and naphthyl phenols 5-8 were investigated by preparative photolyses in CH 3CN-D2O, fluorescence spectroscopy, LFP, and ab initio calculations. ESIPT takes place only in 5 (D-exchange Φ = 0.3), whereas 6-8 undergo solvent-assisted PT with much lower efficiencies. The efficiency of the ESIPT and solvent-assisted PT is mainly determined by different populations of the reactive conformers in the ground state and the NEER principle. The D-exchange experiments and calculations using RI-CC2/cc-pVDZ show that 5 in S1 deactivates by direct ESIPT from the OH to the naphthalene position 1 through a conical intersection with S0, delivering QM 14 that was detected by LFP (τ = 26 ± 3 ns). ESIPT to position 3 in 5 is possible but it proceeds from a less-populated conformer and involves an energy barrier on S1. In solvent-assisted PT to naphthalene position 4 in 5, zwitterion 17 is formed, which cyclizes to stable naphthofuran photoproducts 9-12. The regiochemistry of the deuteration in solvent-assisted PT was correlated with the NBO charges of the corresponding phenolates/naphtholates 5--8-. Combined experimental and theoretical data indicate that solvent-assisted PT takes place via a sequential mechanism involving first deprotonation of the phenol/naphthol, followed by the protonation by H 2O in the S1 state of phenolate/naphtholate. The site of protonation by H2O is mostly at the naphthalene α-position.

A single-step procedure for the preparation of palladium nanoparticles and a phosphine-functionalized support as catalyst for Suzuki cross-coupling reactions

We here report the preparation of supported palladium nanoparticles (NPs) stabilized by pendant phosphine groups by reacting a palladium complex containing the ligand 2-(diphenylphosphino)benzaldehyde with an amino-functionalized silica surface. The Pd na