32884-74-5

Basic information

• Product Name: 1H-Indole, 3-[(4-methylphenyl)thio]-
• CAS NO: 32884-74-5
• Molecular Formula: C15H13NS
• Molecular Weight: 239.341
• Mol File: 32884-74-5.mol
• Article Data: 78

Chemical Properties

• CAS DataBase Reference: 1H-Indole, 3-[(4-methylphenyl)thio]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole, 3-[(4-methylphenyl)thio]-(32884-74-5)
• EPA Substance Registry System: 1H-Indole, 3-[(4-methylphenyl)thio]-(32884-74-5)

Safety Data

• Hazardous Substances Data: 32884-74-5(Hazardous Substances Data)

Upstream product

• 120-72-9 indole 
• 103-19-5 di(p-tolyl) disulfide 
• 106-45-6 para-thiocresol 
• 98-59-9 p-toluenesulfonyl chloride 
• 1576-35-8 toluene-4-sulfonic acid hydrazide 
• 536-57-2 p-toluene sulfinic acid 
• 1858-86-2 Ethyl p-toluenesulfinate 
• 260788-12-3 tert-butyl 2-tosylhydrazine-1-carboxylate 
• 2943-42-2 di(4-methyl)phenylthiosulfonate 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 38078-55-6 sodium S-(4-methylphenyl) thiosulfate 
• 6066-82-6 1-hydroxy-pyrrolidine-2,5-dione 
• 64-17-5 ethanol 
• 1593-60-8 p-toluenesulfonylhydroxylamine 

Downstream Products

• 170499-50-0 1-phenylsulfonyl-3-[(4-(di-tert-butoxycarbonyl)aminomethyl)phenylsulfonyl]indole 
• 170499-49-7 1-phenylsulfonyl-3-[(4-bromomethyl)phenylsulfonyl]indole 
• 170499-51-1 1-phenylsulfonyl-3-[(4-aminomethyl)phenylsulfonyl]indole 
• 170499-48-6 1-phenylsulfonyl-3-(4-methylphenylsulfonyl)indole 
• 170499-47-5 1-Benzenesulfonyl-3-p-tolylsulfanyl-1H-indole 

Relevant articles and documents

Synergistic Effect of Squaric Acid in Bromine-Catalyzed Deoxygenation of Sulfonyl Derivatives: Mechanistic Investigations and Synthetic Applications in Electrophilic (Fluoroalkyl)sulfenylation

A method for electrophilic (fluoroalkyl)sulfenylation of nucleophiles by collaborative CTAB- and squaric acid-promoted deoxygenation of sulfonyl derivatives is reported. Mechanistic studies indicate that squaric acid dramatically decreased the energy barr

Palladium-Catalyzed Direct C2-Biarylation of Indoles

Biaryl and indole units are important structural motifs in several bioactive molecules and functional materials. We have accomplished straightforward access to C2-biarylated indole derivatives through palladium-catalyzed C-H activation strategy with a bro

Recyclable Cellulose-Derived Fe3O4@Pd NPs for Highly Selective C–S Formation by Heterogeneously C–H Sulfenylation of Indoles

Abstract: An efficient and convenient method was developed for the preparation of 3-sulfenylindoles via a cellulose-derived Fe3O4@Pd NPs catalyzed heterogeneously C–H sulfenylation of indoles. This approach provides an effective synthetic route to an important class of indoles derivatives and features high efficiency, easy operation, good practicality, and environmental friendliness. The recoverable catalyst was separated from the reaction mixture using an outside magnetic field and can be recycled five times without huge loss of catalytic performance. Graphic Abstract: An efficient method was developed for the preparation of 3-sulfenylindoles via cellulose-derived Fe3O4@Pd NPs catalyzed heterogeneously C–H sulfenylation of indoles.[Figure not available: see fulltext.].