225668-35-9

Basic information

• Product Name: Ethanone, 2-(4-chlorophenyl)-1-[4-(methylthio)phenyl]-
• CAS NO: 225668-35-9
• Molecular Formula: C15H13ClOS
• Molecular Weight: 276.787
• Mol File: 225668-35-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Ethanone, 2-(4-chlorophenyl)-1-[4-(methylthio)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-(4-chlorophenyl)-1-[4-(methylthio)phenyl]-(225668-35-9)
• EPA Substance Registry System: Ethanone, 2-(4-chlorophenyl)-1-[4-(methylthio)phenyl]-(225668-35-9)

Safety Data

• Hazardous Substances Data: 225668-35-9(Hazardous Substances Data)

Upstream product

• 100-68-5 methyl-phenyl-thioether 
• 25026-34-0 4-chlorophenacetyl chloride 
• 1878-66-6 4-chlorophenylacetic Acid 

Downstream Products

• 177755-50-9 1-(4-chlorophenyl)-2-[4-(methylthio)phenyl]ethane-1,2-dione 
• 1455272-71-5 4-(4-methylthiophenyl)-5-(4-chlorophenyl)-2-(benzylthio)-thiazole 
• 1542256-69-8 C₁₆H₁₂ClN₃O₂S₂ 
• 1542256-64-3 C₁₅H₁₂ClNO₄S 
• 1542256-74-5 5-(4-chlorophenyl)-6-(4-(methylsulfonyl) phenyl)-3-(methylthio)-1,2,4-triazine 
• 1446909-40-5 5-(4-chlorophenyl)-1-methyl-2-(methylthio)-4-(4-(methylthio)phenyl)-1H-imidazole 
• 1415020-22-2 C₁₆H₁₃ClN₂S₂ 
• 1429184-67-7 C₁₆H₁₃ClN₂O₂S₂ 
• 1429184-65-5 C₁₅H₁₃ClO₂S 
• 1429184-64-4 C₁₅H₁₂BrClOS 
• 1429184-80-4 C₁₈H₁₇ClN₂O₄S₂ 
• 1429184-74-6 C₁₈H₁₇ClN₂O₂S₂ 
• 1429184-77-9 C₁₇H₁₅ClN₂O₄S₂ 
• 877224-37-8 C₁₆H₁₆ClN₃O₃S 

Relevant articles and documents

Synthesis, antileukemic and antiplatelet activities of 2,3-diaryl-6,7-dihydro-5H-1,4-diazepines

The synthesis, antileukemic and antiplatelet activity evaluation of 2,3-diaryl-6,7-dihydro-5H-1,4-diazepines are described. In general, it was found that compound 17o showed moderate antileukemic activity against MOLT3 human leukemic cancer cell lines. An arachidonic acid induced platelet aggregation effect on washed rat platelets was studied. Compound 17i was found to be the most potent. The antiplatelet properties may be mediated by interference with the arachidonic acid pathway.

Syntheses of 4,5-diaryl-1,2,3-thiadiazoles

Reaction of thionyl chloride with semicarbazones of 1-(4- methylsulfonylphenyl)-2-(4-substituted pheny)lethanone gave 4-(4- methylsulfonylphenyl)-5-(4-substituted) pheny-1,2,3-thiadiazoles 5. Compounds 5-phenyl-4-(substitutedphenyl)-1,2,3-thiadiazoles 14 were similarly prepared. Chlorosulfonation of the latter followed by ammonia gave the desired compounds 5-(4-aminosulfonylphenyl)-4-(substituted) phenyl-1,2,3-thiadiazoles 6. Copyright Taylor & Francis Inc.