111064-96-1

Basic information

• Product Name: (2-methoxynaphthalen-1-yl)(p-tolyl)sulfane
• Synonyms: (2-methoxynaphthalen-1-yl)(p-tolyl)sulfane
• CAS NO: 111064-96-1
• Molecular Weight: 280.39
• Mol File: 111064-96-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2-methoxynaphthalen-1-yl)(p-tolyl)sulfane(CAS DataBase Reference)
• NIST Chemistry Reference: (2-methoxynaphthalen-1-yl)(p-tolyl)sulfane(111064-96-1)
• EPA Substance Registry System: (2-methoxynaphthalen-1-yl)(p-tolyl)sulfane(111064-96-1)

Safety Data

• Hazardous Substances Data: 111064-96-1(Hazardous Substances Data)

Upstream product

• 93-04-9 2-Methoxynaphthalene 
• 106-45-6 para-thiocresol 
• 98-59-9 p-toluenesulfonyl chloride 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 3401-47-6 1-bromo-2-methoxynaphthalene 
• 10486-08-5 sodium p-thiocresolate 

Downstream Products

• 108980-64-9 1-tosylnaphthalen-2-ol 
• 109251-25-4 2-methoxy-1-(toluene-4-sulfonyl)-naphthalene 

Relevant articles and documents

Direct C-H Thiolation for Selective Cross-Coupling of Arenes with Thiophenols via Aerobic Visible-Light Catalysis

An aerobic metal-free, visible-light-induced regioselective thiolation of phenols with thiophenols is reported. The cross-coupling protocol exhibits great functional group tolerance and high regioselectivity. Mechanistic studies reveal that the disulfide

Acid-induced chemoselective arylthiolations of electron-rich arenes in ionic liquids from sodium arylsulfinates: The reducibility of halide anions in [Hmim]Br

An acid-induced protocol for the chemoselective arylthiolations of electron-rich arenes in ionic liquids from sodium arylsulfinates is introduced. The chemistry, in which [Hmim]Br (heaxylmethylimidazolium bromide) is used as both a solvent and a reducer, provides several advantages including odorless and simple operation, inexpensive reagents, recyclable solvents and gram-scale synthesis.