1666-11-1

Basic information

• Product Name: bis(2,4-dinitrophenyl) diselenide
• Synonyms: bis(2,4-dinitrophenyl) diselenide
• CAS NO: 1666-11-1
• Molecular Weight: 492.122
• Mol File: 1666-11-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: bis(2,4-dinitrophenyl) diselenide(CAS DataBase Reference)
• NIST Chemistry Reference: bis(2,4-dinitrophenyl) diselenide(1666-11-1)
• EPA Substance Registry System: bis(2,4-dinitrophenyl) diselenide(1666-11-1)

Safety Data

• Hazardous Substances Data: 1666-11-1(Hazardous Substances Data)

Upstream product

• 110-86-1 pyridine 
• 67-56-1 methanol 
• 92988-92-6 2,4-dinitrophenyl selenocyanate 
• 127-09-3 sodium acetate 
• 584-48-5 2,4-dinitrobromobenzene 
• 63155-94-2 2,4-dinitro-benzeneselenenyl bromide 
• 113869-17-3 2,4-dinitro-benzeneselenenic acid 
• 97-00-7 1-chloro-2,4-dinitro-benzene 
• 64-17-5 ethanol 
• 65252-77-9 2,4-dinitrobenzeneseleninic acid 

Downstream Products

• 149419-72-7 (Z)-2-((o,p-dinitrophenyl)seleno)-1-(p-toluenesulfonyl)-2-hexene 
• 113869-17-3 2,4-dinitro-benzeneselenenic acid 
• 108787-94-6 2,4-dinitrobenzeneperoxyseleninic acid 
• 65252-77-9 2,4-dinitrobenzeneseleninic acid 
• 63155-94-2 2,4-dinitro-benzeneselenenyl bromide 
• 55382-40-6 trichloro-(2,4-dinitro-phenyl)-λ⁴-selane 

Relevant articles and documents

Synthesis of organic diselenide using zinc powder

A new synthetic method of diselenide by reducing element selenium with zinc powder in basic environment, and then reacting with electrophiles is described. Nine diselenides are synthesized with yields between 52-90%.

LITHIUM DISELENIDE IN APROTIC MEDIUM - A CONVENIENT REAGENT FOR SYNTHESIS OF ORGANIC DISELENIDES

The reduction of selenium with lithium in THF in the presence of diphenylacetylene as a catalyst afforded lithium diselenide, which reacted with electrophiles giving alkyl or aryl diselenides 1 - 3 and selenides 4, as by-products.The useful method for preparation of diselenides based on this reaction was elaborated.