30089-54-4

Basic information

• Product Name: 2-<(2-Methoxyphenyl)thio>-1-phenylethanone
• CAS NO: 30089-54-4
• Molecular Weight: 258.341
• Mol File: 30089-54-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-<(2-Methoxyphenyl)thio>-1-phenylethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-<(2-Methoxyphenyl)thio>-1-phenylethanone(30089-54-4)
• EPA Substance Registry System: 2-<(2-Methoxyphenyl)thio>-1-phenylethanone(30089-54-4)

Safety Data

• Hazardous Substances Data: 30089-54-4(Hazardous Substances Data)

Upstream product

• 2388-73-0 1-methoxy-2-(methylsulfanyl)benzene 
• 98-88-4 benzoyl chloride 
• 100-42-5 styrene 
• 7217-59-6 2-Methoxybenzenethiol 
• 1021-45-0 phosphoric acid diethyl ester-(1-phenyl-vinyl ester) 
• 20718-17-6 2-(dimethyl(oxo)-λ⁶-sulfaneylidene)-1-phenylethan-1-one 

Relevant articles and documents

Air oxidative radical hydroxysulfurization of styrenes leading to β-hydroxysulfides

Air oxidative radical hydroxysulfurization of styrenes initiated by 0.5 mol % of tert-butyl hydroperoxide with arylthiols is described, and a new type of difunctionalization of alkenes was achieved.

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.