68211-49-4

Basic information

• Product Name: 1-Naphthalenol, 4-methylbenzenesulfonate
• CAS NO: 68211-49-4
• Molecular Formula: C17H14O3S
• Molecular Weight: 298.362
• Mol File: 68211-49-4.mol
• Article Data: 31

Chemical Properties

• CAS DataBase Reference: 1-Naphthalenol, 4-methylbenzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Naphthalenol, 4-methylbenzenesulfonate(68211-49-4)
• EPA Substance Registry System: 1-Naphthalenol, 4-methylbenzenesulfonate(68211-49-4)

Safety Data

• Hazardous Substances Data: 68211-49-4(Hazardous Substances Data)

Usage

Type of compound

Sulfonated derivative of 1-naphthalenol

Structure

Naphthalene ring and a methylbenzene sulfonate group

Uses

Production of pharmaceuticals, pesticides, and dyes; intermediate in the synthesis of various organic compounds; reagent in chemical reactions; potential applications in materials science for the production of functional materials and polymers

Handling

Can be hazardous if not properly managed

Upstream product

• 90-15-3 α-naphthol 
• 98-59-9 p-toluenesulfonyl chloride 
• 91-20-3 naphthalene 
• 104-15-4 toluene-4-sulfonic acid 
• 4124-41-8 p-toluenesulfonylanhydride 
• 72973-25-2 N,N-dimethyl-1-(p-tolylsulfonyl)pyridin-1-ium-4-amine chloride 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 99747-74-7 1-naphthyl triflate 
• 3019-88-3 sodium naphtholate 

Downstream Products

• 86-53-3 1-Cyanonaphthalene 
• 27331-33-5 1-(4-methoxyphenyl)naphthalene 
• 728919-25-3 3-(naphthalen-1-yl)aniline 
• 93321-11-0 1-(2-methoxyphenyl)naphthalene 
• 229467-26-9 4-naphthalene-1-ylbenzoic acid methyl ester 
• 604-53-5 1,1'-bisnaphthalene 
• 3042-69-1 1-cyclohexylnaphthalene 
• 173300-93-1 1-(2,6-dimethoxyphenyl)naphthalene 
• 605-02-7 1-phenylnaphthalene 
• 134-32-7 1-amino-naphthalene 
• 27331-34-6 1-(4-methylphenyl)naphthalene 
• 27331-37-9 4-(naphthalen-1-yl)benzonitrile 
• 27331-44-8 1-(3-methylphenyl)naphthalene 
• 840541-78-8 (2,3-dimethylphenyl)-naphthalen-1-yl-amine 

Relevant articles and documents

Application of 1-sulfonyl naphthol derivative in prevention and treatment of plant pathogenic fungi and antibacterial agent

The invention relates to application of a 1-sulfonyl naphthol derivative in prevention and treatment of plant pathogenic fungi and an antibacterial agent, and belongs to the technical field of antibacterial agents. In the application of the 1-sulfonyl nap

Palladium-Catalyzed Cyclobutanation of Aryl Sulfonates through both C-O and C-H Cleavage

A palladium-catalyzed cyclobutanation of aryl sulfonates with strained alkenes has been developed. The methodology is featured to achieve the cleavage of both C-O and C-H bonds of phenol derivatives in one pot. Under the reaction conditions, in addition t

Copper-Catalyzed Regioselective C-H Sulfonyloxylation of Electron-Rich Arenes with p-Toluenesulfonic Acid and Sulfonyloxylation of Aryl(mesityl)iodonium Sulfonates

Copper-catalyzed regioselective C-H sulfonyloxylation of electron-rich arenes with p-toluenesulfonic acid has been developed. Electron-rich benzene derivatives and heteroarenes can undergo this C-H sulfonyloxylation reaction to generate aryl tosylates. Furthermore, sulfonyloxylation of aryl(mesityl)iodonium sulfonates has also been investigated. Both aryl(mesityl)iodonium tosylates and triflates can react smoothly to get aryl sulfonates. The formed aryl sulfonates can be converted to phenols, as well as used as good partners of cross-coupling reactions.