174715-24-3

Basic information

• Product Name: 5-iodo-1-(4-methylphenylsulfonyl)indole
• Synonyms: 5-iodo-1-(4-methylphenylsulfonyl)indole
• CAS NO: 174715-24-3
• Molecular Weight: 397.236
• Mol File: 174715-24-3.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 5-iodo-1-(4-methylphenylsulfonyl)indole(CAS DataBase Reference)
• NIST Chemistry Reference: 5-iodo-1-(4-methylphenylsulfonyl)indole(174715-24-3)
• EPA Substance Registry System: 5-iodo-1-(4-methylphenylsulfonyl)indole(174715-24-3)

Safety Data

• Hazardous Substances Data: 174715-24-3(Hazardous Substances Data)

Upstream product

• 16066-91-4 5-iodo-1H-indole 
• 98-59-9 p-toluenesulfonyl chloride 
• 20780-76-1 5-iodoisatin 

Downstream Products

• 174715-23-2 5-(α-fluorovinyl)-N-tosylindole 
• 1040526-95-1 methyl (E)-3-(1-tosyl-1H-indol-5-yl)acrylate 
• 1296844-10-4 5-phenyl-1-tosyl-1H-indole 
• 1582807-15-5 (S)-2-phthalimido-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)-3-(1-tosyl-1H-indol-5-yl)propanamide 
• 1579852-47-3 3-(1-tosyl-1H-indol-5-yl)phenol 
• 110073-78-4 methyl 1-tosyl-1H-indole-5-carboxylate 

Relevant articles and documents

C(sp3)-H Monoarylation of Methanol Enabled by a Bidentate Auxiliary

With the assistance of a practical directing group (COAQ), the first catalytic protocol for the palladium-catalyzed C(sp3)-H monoarylation of methanol has been developed, offering an invaluable synthesis means to establish extensive derivatives of crucial arylmethanol functional fragments. Furthermore, the gram-scale reaction, broad substrate scope, excellent functional group compatibility, and even the practical synthesis of medicines further demonstrate the usefulness of this strategy.

Palladium-Catalyzed Chlorocarbonylation of Aryl (Pseudo)Halides Through In Situ Generation of Carbon Monoxide

An efficient palladium-catalyzed chlorocarbonylation of aryl (pseudo)halides that gives access to a wide range of carboxylic acid derivatives has been developed. The use of butyryl chloride as a combined CO and Cl source eludes the need for toxic, gaseous carbon monoxide, thus facilitating the synthesis of high-value products from readily available aryl (pseudo)halides. The combination of palladium(0), Xantphos, and an amine base is essential to promote this broadly applicable catalytic reaction. Overall, this reaction provides access to a great variety of carbonyl-containing products through in situ transformation of the generated aroyl chloride. Combined experimental and computational studies support a reaction mechanism involving in situ generation of CO.

Carbon Dioxide as a Directing Group for C-H Functionalization Reactions Involving Lewis Basic Amines, Alcohols, Thiols, and Phosphines for the Synthesis of Compounds

Methods of synthesizing compounds using CO2 as a directing group for C—H functionalization, and compounds made thereby, are described.