1240390-05-9

Basic information

• Product Name: (4-methoxyphenyl)(2,4,6-trimethylphenyl)iodonium tosylate
• Synonyms: (4-methoxyphenyl)(2,4,6-trimethylphenyl)iodonium tosylate
• CAS NO: 1240390-05-9
• Molecular Weight: 524.42
• Mol File: 1240390-05-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (4-methoxyphenyl)(2,4,6-trimethylphenyl)iodonium tosylate(CAS DataBase Reference)
• NIST Chemistry Reference: (4-methoxyphenyl)(2,4,6-trimethylphenyl)iodonium tosylate(1240390-05-9)
• EPA Substance Registry System: (4-methoxyphenyl)(2,4,6-trimethylphenyl)iodonium tosylate(1240390-05-9)

Safety Data

• Hazardous Substances Data: 1240390-05-9(Hazardous Substances Data)

Upstream product

• 696-62-8 para-iodoanisole 
• 104-15-4 toluene-4-sulfonic acid 
• 108-67-8 1,3,5-trimethyl-benzene 
• 100-66-3 methoxybenzene 
• 33035-41-5 2-(diacetoxyiodo)mesitylene 
• 5720-07-0 4-methoxyphenylboronic acid 
• 657-84-1 sodium tosylate 

Downstream Products

• 61248-61-1 2-(tert-butoxy)-1,3,5-trimethylbenzene 
• 19061-33-7 6-methoxy-1,4-dihydro-1,4-epoxidonaphthalene 

Relevant articles and documents

One-Pot Synthesis of Unsymmetric Diaryliodonium Salts from Iodine and Arenes

The first synthesis of unsymmetric diaryliodonium salts directly from iodine and arenes is presented. The methodology provides diaryliodonium salts with the trimethoxyphenyl (TMP) moiety as dummy group. The protocol avoids the customary use of iodoarenes,

A Selective C?H Deprotonation Strategy to Access Functionalized Arynes by Using Hypervalent Iodine

Described here is an efficient method to access highly functionalized arynes from unsymmetrical aryl(mesityl)iodonium tosylate salts. The iodonium salts are prepared in a single pot from either commercially available aryl iodides or arylboronic acids. The