72496-80-1

Basic information

• Product Name: 1H-Indole, 3-[(4-nitrophenyl)thio]-
• CAS NO: 72496-80-1
• Molecular Formula: C14H10N2O2S
• Molecular Weight: 270.312
• Mol File: 72496-80-1.mol
• Article Data: 29

Chemical Properties

• CAS DataBase Reference: 1H-Indole, 3-[(4-nitrophenyl)thio]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole, 3-[(4-nitrophenyl)thio]-(72496-80-1)
• EPA Substance Registry System: 1H-Indole, 3-[(4-nitrophenyl)thio]-(72496-80-1)

Safety Data

• Hazardous Substances Data: 72496-80-1(Hazardous Substances Data)

Upstream product

• 120-72-9 indole 
• 1849-36-1 para-nitrobenzenethiol 
• 2937-05-5 4-nitrobenzenesulfonohydrazide 
• 13165-85-0 ethyl p-nitrobenzenesulphinate 
• 100-00-5 4-chlorobenzonitrile 
• 636-98-6 p-nitrobenzene iodide 
• 51221-38-6 N-hydroxy-4-nitrobenzenesulfonamide 
• 98-74-8 4-Nitrobenzenesulfonyl chloride 
• 17796-89-3 1-[(4-nitrophenyl)sulfanyl]pyrrolidine-2,5-dione 
• 1199-67-3 4-nitro-benzenesulfinic acid 
• 100-32-3 di(p-nitrophenyl) disulfide 
• 937-32-6 4-nitrobenzenesulfenyl chloride 

Relevant articles and documents

A rapid synthesis of 3-sulfenyl indoles using Selectfluor

The direct 3-arylthiolation of indoles with aromatic thiols has been achieved in the presence of Selectfluor under mild conditions to produce 3-arylthioindoles in relatively good to excellent yields and with high selectivity. This method is effective even

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

Cuprous complex, preparation method thereof and application of cuprous complex in synthesis of 3-indolyl thioether

The invention relates to a cuprous complex, a preparation method thereof and an application of the cuprous complex in synthesis of 3-indolyl thioether. The structural formula of the cuprous complex isshown in the specification, Ar is aryl containing a benzene ring or heterocyclic aryl, and ''.'' is a boron hydrogen bond; the preparation method comprises the following steps: 1) dissolving ortho-carborane diformaldehyde and arylamine in an organic solvent, reacting at 60-100 DEG C, and cooling to room temperature after the reaction is finished; and 2) adding CuI, reacting at room temperature for 3-6 hours, and separating to obtain the cuprous complex. Compared with the prior art, the cuprous complex containing the ortho-position carborane Schiff base ligand can efficiently catalyze the coupling reaction of synthesizing a 3-indolyl thioether compound from indole and thiophenol, the method has the advantages of high selectivity, low catalyst dosage, mild reaction conditions, open reaction(taking air as an oxidant), high reaction rate, high yield, wide substrate range and the like and shows a wide industrial application prospect.