973-18-2

Basic information

• Product Name: Benzene, 1,1'-selenobis[2,3,4,5,6-pentafluoro-
• CAS NO: 973-18-2
• Molecular Formula: C12F10Se
• Molecular Weight: 413.076
• Mol File: 973-18-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzene, 1,1'-selenobis[2,3,4,5,6-pentafluoro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-selenobis[2,3,4,5,6-pentafluoro-(973-18-2)
• EPA Substance Registry System: Benzene, 1,1'-selenobis[2,3,4,5,6-pentafluoro-(973-18-2)

Safety Data

• Hazardous Substances Data: 973-18-2(Hazardous Substances Data)

Upstream product

• 18064-78-3 bis(pentafluorophenyl)diselane 
• 18064-76-1 bis(pentafluorophenyl)telluride 
• 7782-49-2 selenium 
• 827-15-6 1,2,3,4,5-pentafluoro-6-iodobenzene 
• 1206-46-8 trimethyl(pentafluorophenyl)silane 
• 40586-75-2 pentafluoroselenoanisole 
• 18064-83-0 tetrakis(pentafluorophenyl)tellurium(IV) 
• 1076-44-4 pentafluorophenyl lithium 
• 973-17-1 bis(pentafluorophenyl)mercury(II) 
• 879-05-0 2,3,4,5,6-pentafluorophenylmagnesium bromide 
• 10026-03-6 selenium tetrachloride 
• 363-72-4 Pentafluorobenzene 
• 7783-70-2 antimony pentafluoride 
• 462-06-6 fluorobenzene 

Downstream Products

• 122183-95-3 C₁₂F₁₂Se 
• 1043-50-1 pentafluorophenyl sulfide 
• 434-90-2 decafluorobiphenyl 
• 18707-14-7 bis(pentafluorophenyl) sulphone 
• 967-95-3 1,1′-sulfanediylbis(2,3,5,6-tetrafluorobenzene) 

Relevant articles and documents

Catalysis with Pnictogen, Chalcogen, and Halogen Bonds

Halogen- and chalcogen-based σ-hole interactions have recently received increased interest in non-covalent organocatalysis. However, the closely related pnictogen bonds have been neglected. In this study, we introduce conceptually simple, neutral, and mon

Oxidative perfluoroorganylation methods in group 12-16 chemistry: The reactions of haloperfluoroorganics and In and InBr, a convenient new route to AgRf (Rf = CF3, C6F5) and reactions of AgRf

Perfluoroiodo organics RfI (Rf = n-CnF2n+1 (n = 1, 2, 3, 4, 6), i-C3F7, C6F5) and C6F5Br react with elemental indium in polyethers or THF to give

POSSIBILITY OF USING ANTIMONY PENTAFLUORIDE INTERCALATED IN GRAPHITE AS CATALYSTS FOR REACTIONS OF THE FRIEDEL-CRAFTS TYPE

Antimony pentafluoride intercalated in graphite, produced by the reaction of gaseous antimony pentafluoride with powdered graphite in a flow-type system at 140-160 deg C, exhibits the characteristics of liquid antimony pentafluoride in the temperature range of 50-100 deg C and can be used as a catalyst for various processes of the Friedel-Crafts type.The alkylation (by 1-bromooctane, cyclohexene, cyclopentene, and acylation by capryloyl, benzoyl, and perfluorobutyryl chlorides) of benzene were realized.The oxidative characteristics of antimony pentafluoride were used for the generation of the polyatomic doubly charged sulfur cation and electrophilic reagents from polyfluorodiaryl disulfide, lead thiocyanate, and mercuric oxide and their introduction into reaction with benzene.