79388-20-8

Basic information

• Product Name: 3-(methylthio)-1-phenylindolin-2-one
• Synonyms: 3-(methylthio)-1-phenylindolin-2-one
• CAS NO: 79388-20-8
• Molecular Weight: 255.34
• Mol File: 79388-20-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-(methylthio)-1-phenylindolin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(methylthio)-1-phenylindolin-2-one(79388-20-8)
• EPA Substance Registry System: 3-(methylthio)-1-phenylindolin-2-one(79388-20-8)

Safety Data

• Hazardous Substances Data: 79388-20-8(Hazardous Substances Data)

Upstream product

• 79388-14-0 N-phenyl-α-(methylthio)acetanilide 
• 624-92-0 Dimethyldisulphide 
• 122-39-4 diphenylamine 
• 79388-13-9 α-chloro-α-(methylthio)-acetyl chloride 
• 79388-17-3 diphenyl methyl sulfinylacetamide 

Downstream Products

• 3335-98-6 1-phenyl-1,3-dihydro-indol-2-one 

Relevant articles and documents

Rhodium(II)-catalyzed direct sulfenylation of diazooxindoles with disulfides

Rhodium(ii)-catalyzed direct sulfenylation of diazooxindoles using disulfides as the sulfenylating agent was developed via intermolecular C-S bond formation. This novel protocol provides a rapid synthetic route to 3-alkylthiooxindoles, 3,3-dialkylthiooxindoles, or 3,3-diarylthiooxindoles in moderate to good yield. The transformation is proposed to proceed through sulfur ylide formation followed by S-S bond cleavage and rearrangement.

Pummerer-Type Reaction of α-Acylsulfides Using Phenyl Iodosyl Bis(trifluoroacetate)

Treatment of α-acylsulfides with phenyl iodosyl bis(trifluoroacetate) (PIFA) resulted in a Pummerer type reaction to give the same products as obtained by the Pummerer reaction of the α-acylsulfoxides.The Pummerer-type reaction of α-acylsulfides using PIF