2874-94-4

Basic information

• Product Name: tris-(pentafluoro phenyl) bromo stannane
• CAS NO: 2874-94-4
• Molecular Weight: 699.788
• Mol File: 2874-94-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: tris-(pentafluoro phenyl) bromo stannane(CAS DataBase Reference)
• NIST Chemistry Reference: tris-(pentafluoro phenyl) bromo stannane(2874-94-4)
• EPA Substance Registry System: tris-(pentafluoro phenyl) bromo stannane(2874-94-4)

Safety Data

• Hazardous Substances Data: 2874-94-4(Hazardous Substances Data)

Upstream product

• 879-05-0 2,3,4,5,6-pentafluorophenylmagnesium bromide 
• 1755-63-1 tris-(pentafluoro phenyl) chloro stannane 
• 1065-49-2 perfluoro(tetraphenyl)tin 
• 7789-67-5 stannic bromide 
• 653-38-3 (pentafluoro phenyl) methyl mercury 
• 7726-95-6 bromine 

Downstream Products

• 40171-35-5 bis-{tris-(pentafluoro phenyl) stannyl} mercury 
• 34664-57-8 hexakis-(pentafluoro phenyl) distannane 
• 69656-73-1 (C₆F₅)3Sn(C₂H₅) 
• 52057-33-7 tris-(pentafluoro phenyl) tin trifluoro acetate 
• 40170-60-3 {Tris-(pentafluoro phenyl) stannyl} {tris-(pentafluoro phenyl) germyl} mercury 
• 54600-47-4 tris-{(pentafluoro phenyl) germyl} tris-{(pentafluoro phenyl) stannyl} sulfane 
• 54600-48-5 tris-{(pentafluoro phenyl) germyl} tris-{(pentafluoro phenyl) stannyl} selane 
• 34727-15-6 bis-{tris-(pentafluoro phenyl) stannyl} sulfane 
• 1262-57-3 (C₆F₅)3Sn(C₆H₅) 
• 34740-24-4 bis-{tris-(pentafluoro phenyl) stannyl} tellane 
• 34727-16-7 bis-{tris-(pentafluoro phenyl) stannyl} selane 

Relevant articles and documents

Preparation, reactivities, and NMR spectra of pentafluorophenyltin derivatives

A variety of pentafluorophenyltin compounds were prepared and their chemical properties were examined. These compounds effectively catalyzed Mukaiyama-aldol reaction of ketene silyl acetal in sharp contrast to the inertness of normal alkyltin halides like Bu2SnCl2. The increased Lewis acidity of the pentafluorophenyltin halides was proved by 119Sn- and 13C-NMR spectra. On the other hand, the pentafluorophenyl group reduced the reactivities of tin towards both nucleophiles and electrophiles. 19F-NMR spectroscopy was invoked to elucidate this anomaly.