59919-12-9

Basic information

• Product Name: 1-Pentanone, 1-phenyl-2-(phenylthio)-
• Synonyms: 1-Phenyl-2-phenylthiopentan-1-one;Phenyl (1-Phenylthio)butyl ketone;1-Pentanone,1-phenyl-2-(phenylthio)
• CAS NO: 59919-12-9
• Molecular Formula: C17H18OS
• Molecular Weight: 270.395
• Mol File: 59919-12-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-Pentanone, 1-phenyl-2-(phenylthio)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Pentanone, 1-phenyl-2-(phenylthio)-(59919-12-9)
• EPA Substance Registry System: 1-Pentanone, 1-phenyl-2-(phenylthio)-(59919-12-9)

Safety Data

• Hazardous Substances Data: 59919-12-9(Hazardous Substances Data)

Upstream product

• 49851-31-2 α-bromovalerophenone 
• 931-59-9 benzenesulfenyl chloride 
• 1009-14-9 phenyl butyl ketone 
• 98-88-4 benzoyl chloride 
• 108-98-5 thiophenol 
• 72653-47-5 α-chlorobutyl phenyl sulfide 

Downstream Products

• 95607-26-4 1-phenyl-2-phenylsulphinylpentan-1-one 
• 109328-60-1 (E)-1-phenyl-2-phenylthiopent-3-en-1-on 
• 109328-59-8 (E)-2-methyl-1-phenyl-2-phenylthiopent-3-en-1-one 
• 95607-29-7 1-phenyl-2-phenylthiopent-2-en-1-one 
• 109328-52-1 (E)-1-phenyl-2-phenylthiopent-2-en-1-one 
• 98793-56-7 (Z)-1-phenyl-2-phenylthiopent-2en-1-one 

Relevant articles and documents

Copper-catalyzed cross-coupling reaction of α-sulfur-substituted alkylstannanes with acid chlorides

Copper compounds were found to catalyze the cross-coupling reaction of α-sulfur-substituted alkylstannanes with acid chlorides. Under the optimized conditions (CuF2 (1 mol %), 1,4-dioxane, 102 C), various substrates coupled to afford the corres

Preparation and reactivity of polyfunctional zinc and copper organometallics bearing sulfur functionalities

Iodomethylthiobenzoate 5 and α-chloroalkyl phenyl sulfides 6 were found to insert zinc dust in THF under very mild conditions (10-25°C, 0.5-2 h) leading to zinc α-thioorganometallics. After a transmetallation with CuCN·2 LiCl, the corresponding copper rea

Synthesis of α-Phenylthio Enones and Esters of α-Phenylthio Alkenoic Acids

The title compounds can be made by a Pummerer dehydration from the corresponding saturated sulphoxides.The alkylation of anions from saturated and unsaturated ketones is described.