53060-07-4

Basic information

• Product Name: 1-methoxy-4-(1,2,2-triiodovinyl)benzene
• Synonyms: 1-methoxy-4-(1,2,2-triiodovinyl)benzene
• CAS NO: 53060-07-4
• Molecular Weight: 511.867
• Mol File: 53060-07-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-methoxy-4-(1,2,2-triiodovinyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methoxy-4-(1,2,2-triiodovinyl)benzene(53060-07-4)
• EPA Substance Registry System: 1-methoxy-4-(1,2,2-triiodovinyl)benzene(53060-07-4)

Safety Data

• Hazardous Substances Data: 53060-07-4(Hazardous Substances Data)

Upstream product

• 2227-57-8 3-(4-methoxyphenyl)propynoic acid 
• 3989-14-8 (4-methoxyphenylethynyl)trimethylsilane 
• 768-60-5 4-methoxyphenylacetylen 
• 696-62-8 para-iodoanisole 
• 7515-17-5 methyl 3-(4-methoxyphenyl)propynoate 

Relevant articles and documents

Oxidant- and additive-free simple synthesis of 1,1,2-triiodostyrenes by one-pot decaroboxylative iodination of propiolic acids

A metal- and oxidant-free facile synthesis of a range of 1,1,2-triiodostryrene derivatives has been developed which utilizes a simple decarboxylative triiodination of propiolic acids using molecular iodine and sodium acetate in a one-pot manner. Electron-

Hypervalent Iodine Mediated Chemoselective Iodination of Alkynes

Reported herein are practical approaches for the chemoselective mono-, di-, and tri-iodination of alkynes based on efficient oxidative iodinations catalyzed by hypervalent iodine reagents. The reaction conditions were systematically optimized by altering

A study on reactions of an alkynylsilane with oxone-KX (X = Cl, Br, I) and its one-pot transformation into an amide/ester

Oxyhalogenation reactions of a variety of alkynylsilanes were studied using oxone as mild oxidant and KCl, KBr, and KI as halogen sources. In this study, reaction of an alkynylsilane with oxone-KX (X = Cl or Br) produced trichloromethyl/tribromomethyl ketones inhigh yields. Under similar conditions, however, reactions of alkynylsilanes with oxone-KI were found to give exclusively 1,2,2-triiodovinyl derivatives in high yields. In this study, new methods were deveoped for effcient one-pot tranformation of alkynylsilanes into amides and esters by reaction with amines and alcohols respectively via trihalomethyl ketone.