452962-71-9

Basic information

• Product Name: 1H-Indole, 3-iodo-1-methyl-2-phenyl-
• CAS NO: 452962-71-9
• Molecular Formula: C15H12IN
• Molecular Weight: 333.171
• Mol File: 452962-71-9.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 1H-Indole, 3-iodo-1-methyl-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole, 3-iodo-1-methyl-2-phenyl-(452962-71-9)
• EPA Substance Registry System: 1H-Indole, 3-iodo-1-methyl-2-phenyl-(452962-71-9)

Safety Data

• Hazardous Substances Data: 452962-71-9(Hazardous Substances Data)

Upstream product

• 3558-24-5 1-methyl-2-phenyl-1H-indole 
• 948-65-2 2-phenyl-indole 
• 536-74-3 phenylacetylene 
• 51234-11-8 3-iodo-2-phenyl-1H-indole 
• 74-88-4 methyl iodide 
• 874770-31-7 N-cyclohexyl-N-methyl-2-(phenylethynyl)aniline 
• 54655-08-2 N,N-dimethyl-2-(2-phenylethynyl)aniline 

Downstream Products

• 1175540-21-2 2-methyl-4-(1-methyl-2-phenyl-indol-3-yl)but-3-yn-2-ol 
• 6121-45-5 1-methyl-2,3-diphenyl-1H-indole 

Relevant articles and documents

Oxone-mediated halocyclization/demethylation of 2-alkynylthioanisoles with sodium halides towards 3-halobenzo[b]thiophenes

An efficient and practical protocol for the Oxone-mediated halocyclization/demethylation of 2-alkynylthioanisoles towards valuable 3-halobenzo[b]thiophenes is described. Structurally diverse 3-halobenzothiophenes were obtained in good to excellent yields

MANUFACTURING METHOD OF AROMATIC IODINE COMPOUND USING DISULFIDE AS CATALYST

To manufacture an aromatic iodine compound under a mild condition at low cost and high yield.SOLUTION: There is provided a manufacturing method of an aromatic iodine compound by reacting an aromatic compound and an iodination agent in a presence of a cata

Disulfide-Catalyzed Iodination of Electron-Rich Aromatic Compounds

Herein, a disulfide-catalyzed electrophilic iodination of aromatic compounds using 1,3-diiodo-5,5-dimethylhydantoin (DIH) has been developed. The disulfide activates DIH as a Lewis base to promote the iodination reaction in acetonitrile under mild conditions. This system is applicable to a wide range of electron-rich aromatic compounds, including acetanilide, anisole, imidazole, and pyrazole derivatives.