21388-17-0

Basic information

• Product Name: 6-ETHYL-2-METHOXYLNAPHTHALINE
• Synonyms: 6-ETHYL-2-METHOXYLNAPHTHALINE;2-Methoxy-6-ethylnaphthalene;Naproxen EP IMpurity J;2-Methoxy-6-ethylnapthalene;Naphthalene,2-ethyl-6-Methoxy-;6-ETHYL-2-METHOXYLPHTHALINE
• CAS NO: 21388-17-0
• Molecular Formula: C₁₃H₁₄O
• Molecular Weight: 201.2643
• Mol File: 21388-17-0.mol
• Article Data: 1

Chemical Properties

• Melting Point: 57-58℃
• Boiling Point: 302℃
• Flash Point: 118℃
• Appearance: /
• Density: 1.032
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: Chloroform (Slightly), Methanol (Slightly)
• CAS DataBase Reference: 6-ETHYL-2-METHOXYLNAPHTHALINE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-ETHYL-2-METHOXYLNAPHTHALINE(21388-17-0)
• EPA Substance Registry System: 6-ETHYL-2-METHOXYLNAPHTHALINE(21388-17-0)

Safety Data

• Hazardous Substances Data: 21388-17-0(Hazardous Substances Data)

Usage

Uses

2-Methoxy-6-ethylnapthalene is a photoproduct of the NSAID Naproxen (N377525).

Upstream product

• 5747-23-9 2-phenyl-1,3,2-benzodioxaborole 
• 129113-00-4 2-ethynyl-6-methoxynaphthalene 

Downstream Products

• 1999-64-0 6-ethyl-2-naphthol 
• 37436-25-2 6-ethyl-3,4-dihydro-2-naphthalinone 
• 23981-80-8 naproxen 
• 31220-35-6 (S)-6-methoxy-α-methyl-2-naphthaleneacetic acid ethyl ester 
• 22204-53-1 (2S)-2-(6-methoxy(2-naphthyl))propanoic acid 
• 612-94-2 2-phenylnaphthalene 
• 1016160-95-4 2-ethyl-6-phenylnaphthalene 
• 102549-01-9 3-(6-ethyl-2-methoxy-[1]naphthyl)-2-phenyl-acrylonitrile 
• 102242-26-2 8-ethyl-2-phenyl-benzo[f]chromen-3-one 
• 63021-34-1 3-ethyl-dibenz[a,h]acridine 
• 14461-83-7 1-Methyl-6-ethyl-naphthol-(2) 

Relevant articles and documents

Enhanced Reactivity of Aerobic Diimide Olefin Hydrogenation with Arylboronic Compounds: An Efficient One-Pot Reduction/Oxidation Protocol

A catalyst-free and efficient method for simultaneous olefin hydrogenation and oxidation of arylboronate esters to phenols with hydrazine hydrate and molecular oxygen is presented. The process is based on the utilization of a readily available Lewis acidic arylboron compound, which evades common problems associated with the catalyst-free aerobic hydrogenation of olefins with diimide. Using an operationally simple procedure, the protocol smoothly delivers phenol derivatives and various alkanes in excellent yields with remarkable functional group compatibility. The method allows the reaction to be scaled up to 1 g of the starting materials.