15161-04-3

Basic information

• Product Name: naphthalen-1-yl benzenesulfonate
• Synonyms: 1-naphthalenol, benzenesulfonate; 1-Naphthyl benzenesulfonate; Benzenesulfonic acid, 1-naphthyl ester
• CAS NO: 15161-04-3
• Molecular Formula: C₁₆H₁₂O₃S
• Molecular Weight: 284.3297
• Mol File: 15161-04-3.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 469.8°C at 760 mmHg
• Flash Point: 237.9°C
• Density: 1.308g/cm³
• Vapor Pressure: 1.51E-08mmHg at 25°C
• Refractive Index: 1.653
• CAS DataBase Reference: naphthalen-1-yl benzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: naphthalen-1-yl benzenesulfonate(15161-04-3)
• EPA Substance Registry System: naphthalen-1-yl benzenesulfonate(15161-04-3)

Safety Data

• Hazardous Substances Data: 15161-04-3(Hazardous Substances Data)

Upstream product

• 108-98-5 thiophenol 
• 90-15-3 α-naphthol 
• 98-09-9 benzenesulfonyl chloride 
• 4106-18-7 1-(phenylsulfonyl)-1H-benzo[d][1,2,3]triazole 
• 3019-88-3 sodium naphtholate 

Downstream Products

• 86-53-3 1-Cyanonaphthalene 
• 605-02-7 1-phenylnaphthalene 
• 3198-32-1 benzenesulfonate 
• 90-15-3 α-naphthol 
• 27331-33-5 1-(4-methoxyphenyl)naphthalene 
• 27331-34-6 1-(4-methylphenyl)naphthalene 
• 91-20-3 naphthalene 

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

One-pot tandem reactions for direct conversion of thiols and disulfides to sulfonic esters, and Paal-Knorr synthesis of pyrrole derivatives catalyzed by TCCA

A convenient synthesis of sulfonic esters from thiols and disulfides is described. In situ preparation of sulfonyl chlorides from thiols is accomplished by oxidation with trichloroisocyanuric acid (TCCA), tetra-butylammonium chloride (t-Bu4NCl), and water. The sulfonyl chlorides are then further allowed to react with phenol derivatives in the same reaction vessel. Also, a facile synthesis of N-substituted pyrroles by the reaction of hexane-2,5-dione with primary amines has been accomplished using TCCA as a catalyst under mild condition with excellent yields.

Highly efficient Pd-catalyzed cyanation of aryl chlorides and arenesulfonates with potassium ferrocyanide in aqueous media

A highly improved Pd-catalyzed cyanation of aryl chlorides to corresponding benzonitriles was demonstrated in aqueous media. Moreover, Pd-catalyzed cyanation of aryl tosylates and benzenesulfonates with K4[Fe(CN) 6] was developed under the similar conditions, which extended application scope of the cyanation. Graphical Abstract: [Figure not available: see fulltext.]