477761-10-7

Basic information

• Product Name: Ethanone, 2-[(4-methylphenyl)thio]-1-(2-naphthalenyl)-
• CAS NO: 477761-10-7
• Molecular Formula: C19H16OS
• Molecular Weight: 292.401
• Mol File: 477761-10-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Ethanone, 2-[(4-methylphenyl)thio]-1-(2-naphthalenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-[(4-methylphenyl)thio]-1-(2-naphthalenyl)-(477761-10-7)
• EPA Substance Registry System: Ethanone, 2-[(4-methylphenyl)thio]-1-(2-naphthalenyl)-(477761-10-7)

Safety Data

• Hazardous Substances Data: 477761-10-7(Hazardous Substances Data)

Upstream product

• 2949-26-0 2-ethynylnaphthalene 
• 106-45-6 para-thiocresol 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 93-08-3 methyl 2-naphthyl ketone 
• 613-54-7 2-Bromo-2'-acetonaphthone 

Relevant articles and documents

Electrocatalytic Synthesis of gem -Bisarylthio Enamines and α-Phenylthio Ketones via a Radical Process under Mild Conditions

The novel method for the synthesis of gem -bisarylthio enamines and α-phenylthio ketones was developed via the coupling of α-substituted vinyl azides with thiols in the presence of tetrabutylammonium iodide (TBAI) as a redox catalyst and electrolyte at ro

Catalyst-Free Difunctionalization of Activated Alkenes in Water: Efficient Synthesis of β-Keto Sulfides and Sulfones

Difunctionalization of activated alkenes, a powerful strategy in chemical synthesis, has been accomplished for direct synthesis of a series of β-keto sulfides and β-keto sulfones. The transformation, mediated by O2, proceeds smoothly in water and without any catalyst. Prominent advantages of this method include mild reaction conditions, purification simplicity, and gram-scale synthesis, underlining the practical utility of this methodology.