1416276-98-6

Basic information

• Product Name: bis(3-methylphenyl)iodonium trifluoromethanesulfonate
• Synonyms: bis(3-methylphenyl)iodonium trifluoromethanesulfonate
• CAS NO: 1416276-98-6
• Molecular Weight: 458.24
• Mol File: 1416276-98-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: bis(3-methylphenyl)iodonium trifluoromethanesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: bis(3-methylphenyl)iodonium trifluoromethanesulfonate(1416276-98-6)
• EPA Substance Registry System: bis(3-methylphenyl)iodonium trifluoromethanesulfonate(1416276-98-6)

Safety Data

• Hazardous Substances Data: 1416276-98-6(Hazardous Substances Data)

Upstream product

• 1493-13-6 trifluorormethanesulfonic acid 
• 19169-97-2 m-(diacetoxyiodo)toluene 
• 17933-03-8 m-tolylboronic acid 
• 625-95-6 3-Iodotoluene 
• 108-88-3 toluene 

Downstream Products

• 60544-09-4 2-(3-methylphenyl)-1,4-naphthoquinone 
• 93504-10-0 2-m-tolylcyclohexa-2,5-diene-1,4-dione 
• 253342-48-2 4,4,5,5-tetramethyl-2-m-tolyl-1,3,2-dioxaborolane 
• 1450884-28-2 m-methylphenyl 4,6-di-O-acetyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside 
• 1315277-67-8 4,4,5,5-tetramethyl-2-(2-m-tolylvinyl)[1,3,2]dioxaborolane 
• 13511-11-0 3-methyl-N-phenyl-N-(m-tolyl)aniline 
• 893752-56-2 2-(m-tolyloxy)benzaldehyde 

Relevant articles and documents

Direct Copper-Catalyzed C-3 Arylation of Diphenylphosphine Oxide Indoles

We have developed a simple and effective method for the C-3 arylation of phosphorus-containing indole compounds in the presence of CuI under mild conditions. This reaction provides a reliable method for the modification of ligands.

Palladium(ii)-catalyzed stereoselective synthesis of: C-glycosides from glycals with diaryliodonium salts

An efficient palladium(ii) mediated C-glycosylation of glycals with diaryliodonium salts is described, providing a new strategy for the synthesis of 2,3-dideoxy C-Aryl glycosides with excellent stereoselectivity. The C-glycosylation of a diverse range of

A mild carbon-boron bond formation from diaryliodonium salts

The direct metal-free borylation of diaryliodonium salts with diboron reagents is now demonstrated to be a feasible process toward formation of aryl boronic esters without any additive or catalysts, and it can be extended to a two-step C-C coupling of both aryl groups of the initial diaryliodonium reagent.