31383-34-3

Basic information

• Product Name: 2-Propanone, 1-(methylsulfinyl)- (7CI,8CI,9CI)
• Synonyms: 2-Propanone, 1-(methylsulfinyl)- (7CI,8CI,9CI)
• CAS NO: 31383-34-3
• Molecular Formula: C₄H₈O₂S
• Molecular Weight: 120.17012
• Product Categories: ACETYLGROUP
• Mol File: 31383-34-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Propanone, 1-(methylsulfinyl)- (7CI,8CI,9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propanone, 1-(methylsulfinyl)- (7CI,8CI,9CI)(31383-34-3)
• EPA Substance Registry System: 2-Propanone, 1-(methylsulfinyl)- (7CI,8CI,9CI)(31383-34-3)

Safety Data

• Hazardous Substances Data: 31383-34-3(Hazardous Substances Data)

Upstream product

• 14109-72-9 methylsulfanyl-acetone 

Downstream Products

• 73121-26-3 1-(2-Phenyl-ethanesulfinyl)-propan-2-one 
• 1363807-81-1 1-[2-(2,6-diethyl-4-methylphenyl)-2-oxoacetyl]-1-methyl-2-(1-methylsulfinyl-2-propylidene)hydrazine 

Relevant articles and documents

METHOD FOR PRODUCING PYRIDAZINONE COMPOUNDS AND INTERMEDIATE THEREOF

The present invention relates to a novel method for producing a pyridazinone compound and an intermediate thereof as shown in the following scheme: wherein the symbols are as defined in the specification.

Selective and mild oxidation of sulfides to sulfoxides by oxodiperoxo molybdenum complexes adsorbed onto silica gel

Aliphatic and aromatic sulfides, ketosulfides, sulfinyl acids and esters, and olefinic sulfides were oxidized to sulfoxides using oxodiperoxo complexes of molybdenum coated on silica gel (150 ? pore size) in very high yields. Complete chemoselectivity was observed for the oxidation of all functional sulfides. Sulfones were, however, the main products of the reaction when the complexes were not coated on silica gel. The influence of silica gel as the support of these reactions was also investigated and it was demonstrated that it alters the reactivity of the complex but it is not responsible for the excellent chemoselectivity of the complexes. The complex [MoO(O2)2(pyrazole) (H2O)] proved to be more reactive than [MoO(O2)2(Opyr) (H2O)].