914930-12-4

Basic information

• Product Name: 4-iodobenzenesulfonic acid methyl ester
• Synonyms: 4-iodobenzenesulfonic acid methyl ester
• CAS NO: 914930-12-4
• Molecular Weight: 298.101
• Mol File: 914930-12-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-iodobenzenesulfonic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-iodobenzenesulfonic acid methyl ester(914930-12-4)
• EPA Substance Registry System: 4-iodobenzenesulfonic acid methyl ester(914930-12-4)

Safety Data

• Hazardous Substances Data: 914930-12-4(Hazardous Substances Data)

Upstream product

• 591-50-4 iodobenzene 
• 77-78-1 dimethyl sulfate 
• 67-56-1 methanol 
• 98-61-3 p-Iodobenzenesulfonyl chloride 

Downstream Products

• 1046799-20-5 (+/-)-N-{2-[4-(2-hydroxy-3-ethoxypropoxy)phenylcarbamoyl]ethyl}-N-methylpiperidinium p-iodobenzenesulfonate 
• 1046799-11-4 (+/-)-N-{2-[4-(2-hydroxy-3-ethoxypropoxy)phenylcarbamoyl]ethyl}-N-methylpyrrolidinium p-iodobenzenesulfonate 
• 25444-35-3 p-(pentadecafluoroheptyl)benzenesulfonyl chloride 

Relevant articles and documents

Helicity induction in charged poly(phenylacetylene)s bearing various acidic functional groups in water and its mechanism

We investigated the helicity induction in a series of stereoregular cis-transoidal poly-(phenylacetylene)s bearing various acidic functional groups, such as a phosphonic acid and its monoethyl ester (poly-1-H and poly-2-H, respectively), a carboxylic acid

Tagged hypervalent iodine reagents: A new purification concept based on ion exchange through SN2 substitution

(Chemical Equation Presented) The preparation of phenylsulfonate-tagged iodine(III) reagents as well as their use in a novel purification strategy for iodine(III)-promoted reactions is described. The concept is based on ion exchange and is initiated by an azide-promoted SN2-reaction at the alkyl sulfonate followed by trapping of the resulting aryl sulfonate anion with an ion-exchange resin. The concept is successfully proven for Ru-catalyzed oxidations of alcohols, the activation and glycosidatlon of thioglycosides, and the Suarez reaction of pyranoses.