83392-35-2

Basic information

• Product Name: methyl 3-(4-methylphenyl)-3-oxopropanedithioate
• Synonyms: methyl 3-(4-methylphenyl)-3-oxopropanedithioate
• CAS NO: 83392-35-2
• Molecular Weight: 224.348
• Mol File: 83392-35-2.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: methyl 3-(4-methylphenyl)-3-oxopropanedithioate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-(4-methylphenyl)-3-oxopropanedithioate(83392-35-2)
• EPA Substance Registry System: methyl 3-(4-methylphenyl)-3-oxopropanedithioate(83392-35-2)

Safety Data

• Hazardous Substances Data: 83392-35-2(Hazardous Substances Data)

Upstream product

• 41467-27-0 3,3-bis(methylthio)-1-(p-tolyl)prop-2-en-1-one 
• 98-86-2 acetophenone 
• 20365-21-3 methyl 3-oxo-3-phenylpropanedithioate 
• 122-00-9 para-methylacetophenone 
• 2314-48-9 (S,S)-dimethyl trithiocarbonate 

Downstream Products

• 843640-84-6 ethyl 2-{[3-(4-methylphenyl)-3-oxopropanthioyl]amino}acetate 
• 1228956-78-2 3-(4-methylbenzoyl)-8-methoxy-2H-chromene-2-thione 
• 835-71-2 2-(4-methylphenyl)-1,3-benzoxazole 
• 31773-64-5 5-methoxy-2-(p-tolyl)benzo[d]oxazole 
• 16715-75-6 2-(4-methylphenyl)-5-chlorobenzoxazole 
• 619-55-6 para-methylbenzamide 
• 99-94-5 p-Toluic acid 
• 881891-95-8 methyl 2-{[3-(4-methylphenyl)-3-oxopropanthioyl]amino}acetate 
• 1592508-07-0 5-(methylthio)-3-(p-tolyl)-1H-pyrazole 
• 7118-66-3 5-methyl-2-(4-methylphenyl)-1H-benzimidazole 

Relevant articles and documents

Silica-ZnCl2: An efficient and reusable solid catalyst for one pot synthesis of 5-methyl mercaptothiocarbonyl-4-aryl-3- dihydropyrimidin-2(1H)-ones under solvent-free conditions

Synthetic application of Silica-ZnCl2, as an efficient and eco-friendly catalyst for the synthesis of a small library of dihydropyrimidinones is described in this report. The reaction involves a one pot, multicomponent reaction of β-oxodithioca

An efficient transesterification of β-oxodithioesters catalyzed by stannous chloride under solvent-free conditions

Transesterification of β-oxodithioesters catalyzed by stannous chloride under solvent-free condition has been reported for the first time. The short reaction time and good to excellent yields using inexpensive catalysts are attractive features of this synthetic protocol. Copyright

Molecular docking and in vitro antileishmanial evaluation of chromene-2-thione analogues

Leishmaniases are an epidemic in various countries, and the parasite is developing resistance against available drugs. Thus, development of new drugs against Leishmania is an open area of investigation for synthetic organic chemists. To meet this challeng