158956-95-7

Basic information

• Product Name: 2,3,4,5-tetrakis(phenylselenenyl)thiophene
• Synonyms: 2,3,4,5-tetrakis(phenylselenenyl)thiophene
• CAS NO: 158956-95-7
• Molecular Weight: 704.373
• Mol File: 158956-95-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,3,4,5-tetrakis(phenylselenenyl)thiophene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4,5-tetrakis(phenylselenenyl)thiophene(158956-95-7)
• EPA Substance Registry System: 2,3,4,5-tetrakis(phenylselenenyl)thiophene(158956-95-7)

Safety Data

• Hazardous Substances Data: 158956-95-7(Hazardous Substances Data)

Upstream product

• 188290-36-0 thiophene 
• 1666-13-3 diphenyl diselenide 
• 158956-93-5 2,5-bis(phenylselenenyl)thiophene 
• 158956-94-6 2,3,5-tris(phenylselenenyl)thiophene 

Downstream Products

• 28622-61-9 butyl phenyl selenide 

Relevant articles and documents

Electrophilic organic selenium reagents - Protonated seleninic acids as precursors for unsymmetrical aromatic selenides

Arylselenylations of methylbenzenes, methoxybenzenes and thiophene were smoothly achieved with selenenium ions generated by comproportionation of 1:1 mixtures of p-toluenesulfonic acid salts of seleninic acids and the corresponding diselenides. A series of p-toluenesulfonic salts of seleninic acids were prepared by hydrogen peroxide oxidation of the corresponding diselenides in the presence of p-toluenesulfonic acid. Novel 2-(organylseleno)thiophenes were obtained by heating the protonated seleninic acids with a 50-fold excess of thiophene in glacial acetic acid.

Electrophilic Phenylselenenylation of Thiophenes. Synthesis of Poly(phenylseleno)thiophenes.

The phenylselenenyl sulfate, generated from the oxidation of diphenyl diselenide with ammonium persulfate, easily effects electrophilic aromatic substituttion reactions on thiophene, 2-and 3-methylthiophenes and on 3-bromothiophene.The phenylseleno group