87228-53-3

Basic information

• Product Name: Ethanone, 2-[(4-methylphenyl)sulfonyl]-2-(methylthio)-1-phenyl-
• CAS NO: 87228-53-3
• Molecular Formula: C16H16O3S2
• Molecular Weight: 320.433
• Mol File: 87228-53-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Ethanone, 2-[(4-methylphenyl)sulfonyl]-2-(methylthio)-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-[(4-methylphenyl)sulfonyl]-2-(methylthio)-1-phenyl-(87228-53-3)
• EPA Substance Registry System: Ethanone, 2-[(4-methylphenyl)sulfonyl]-2-(methylthio)-1-phenyl-(87228-53-3)

Safety Data

• Hazardous Substances Data: 87228-53-3(Hazardous Substances Data)

Upstream product

• 536-74-3 phenylacetylene 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 28995-88-2 1-methyl-4-((phenylethynyl)sulfonyl)benzene 
• 657-84-1 sodium tosylate 
• 93-89-0 benzoic acid ethyl ester 
• 59662-65-6 methylthiomethyl p-tolyl sulfone 
• 93-99-2 benzoic acid phenyl ester 

Downstream Products

• 13603-60-6 S-methyl 2-oxo-2-phenylethanethioate 
• 107536-13-0 2-Methylsulfanyl-1-phenyl-2-(toluene-4-sulfonyl)-ethanol 
• 774-48-1 (diethoxymethyl)benzene 
• 100-52-7 benzaldehyde 
• 107536-05-0 1-(2-Methoxymethoxy-1-methylsulfanyl-2-phenyl-ethanesulfonyl)-4-methyl-benzene 
• 120113-93-1 2-(methoxymethoxy)-2-phenylethanal 

Relevant articles and documents

Direct and Efficient Synthesis of Sulfonium Acyl Sulfonylmethylide Ylides from Acetylenic Sulfones and Dimethyl Sulfoxide

Bifunctionalized sulfonium ylides - sulfonium acyl sulfonylmethylides - were directly and efficiently prepared from various acetylenic sulfones and aliphatic sulfoxides under heating conditions. The current method features short reaction time, low cost, readily available starting materials, convenient operation, and purification, providing an efficient access to widely applied bifunctionalized sulfonium ylides.

A NOVEL ROUTE FROM A CARBOXYLIC ACID TO A CARBALDEHYDE USING METHYLTHIOMETHYL p-TOLYL SULFONE

A new conversion of a carboxylic ester to a carbaldehyde involing formation and dissociation of a C-C bond at the acyl carbon was accomplished by the use of methylthiomethyl p-tolyl sulfone (1).