109545-72-4

Basic information

• Product Name: DIPHENYL IODONIUM-2-CARBOXYLATE
• Synonyms: SALOR-INT L159824-1EA
• CAS NO: 109545-72-4
• Molecular Formula: C13H9IO2
• Molecular Weight: 324.11
• Mol File: 109545-72-4.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: DIPHENYL IODONIUM-2-CARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: DIPHENYL IODONIUM-2-CARBOXYLATE(109545-72-4)
• EPA Substance Registry System: DIPHENYL IODONIUM-2-CARBOXYLATE(109545-72-4)

Safety Data

• Hazardous Substances Data: 109545-72-4(Hazardous Substances Data)

Upstream product

• 88-67-5 2-Iodobenzoic acid 
• 71-43-2 benzene 
• 109185-34-4 (2-carboxy-phenyl)-phenyl-iodonium ; iodide 
• 304-91-6 o-iodosobenzoic acid 

Downstream Products

• 70817-13-9 1,2,3,4-Tetrakis-pentafluorophenyl-naphthalene 
• 1453081-52-1 2-[5-(2-tert-butoxycarbonylamino-2-methoxycarbonylethyl)-2-methoxyphenylamino]benzoic acid 
• 1325207-34-8 2-((2-carboxyethyl)(3,4,5-trimethoxyphenyl)amino)benzoic acid 
• 1239586-34-5 2-(5-methoxy-2-methylphenylamino)benzoic acid 
• 1239586-35-6 2-(2-cyano-5-methoxyphenylamino)benzoic acid 
• 139677-51-3 1-Nitro-9-oxo-9,10-dihydro-acridine-4-carboxylic acid methyl ester 
• 71507-04-5 1-nitro-9-oxo-9,10-dihydroacridine-4-carboxylic acid 
• 94654-73-6 N-(2-carboxyphenylamino)-6-methoxybenzoic acid 
• 94654-49-6 9-oxo-3-phenyl-9,10-dihydroacridine-4-carboxylic acid 

Relevant articles and documents

Process for preparing n-alkylanilines and n-allylanilines

The present invention relates to a process for the n-alkylation and n-allylation of anilines by bringing the aniline into contact with an alkylating or allylating agent in an organic solvent in a homogeneous liquid phase in the presence of an onium ion and a stoichiometric amount of a non-quaternizable base.

Selective chlorination of ortho-substituted phenols

Ortho-substituted phenolic compounds, e.g., 2,6-dichlorophenol, are selectively chlorinated, e.g., into 2,4,6-trichlorophenol, with gaseous chlorine in either the molten state or in a solvent medium, in the presence of a selectivity-enhancing effective amount of an organic cation.