81607-30-9

Basic information

• Product Name: 2,3,4,5,6-pentafluorophenyldifluorobromane
• Synonyms: 2,3,4,5,6-pentafluorophenyldifluorobromane
• CAS NO: 81607-30-9
• Molecular Weight: 284.959
• Mol File: 81607-30-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,3,4,5,6-pentafluorophenyldifluorobromane(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4,5,6-pentafluorophenyldifluorobromane(81607-30-9)
• EPA Substance Registry System: 2,3,4,5,6-pentafluorophenyldifluorobromane(81607-30-9)

Safety Data

• Hazardous Substances Data: 81607-30-9(Hazardous Substances Data)

Upstream product

• 1206-46-8 trimethyl(pentafluorophenyl)silane 
• 7787-71-5 bromine trifluoride 
• 973-17-1 bis(pentafluorophenyl)mercury(II) 
• 15989-98-7 bis(pentafluorophenyl)cadmium 
• 1799-90-2 bis(pentafluorophenyl)zinc 
• 5272-26-4 trifluoro(pentafluorophenyl)silane 

Downstream Products

• 344-04-7 bromopentafluorobenzene 
• 355-42-0 tetradecafluorohexane 
• 57113-81-2 2,3,3,4,5,6,6-heptafluoro-1-bromo-cyclohexa-1,4-diene 
• 4933-59-9 1-bromo nonafluoro cyclohexene 
• 70557-89-0 3-bromoheptafluorocyclohexa-1,4-diene 

Relevant articles and documents

BEITRAEGE ZUR CHEMIE DES BROMTRIFLUORIDS 1.TEIL PENTAFLUORPHENYLBROM(III)DIFLUORID UND -BIS(TRIFLUORACETAT)

BrF3 reacts with C6F5SiF3 to form C6F5BrF2, a volatile, colourless, and thermally stable solid, which melts at 35 - 36 deg C without decomposition.Its chemical and spetroscopic properties are in contrast to the product described by Sams .The reactivity

Contributions to the chemistry of brominetrifluoride. Part 2. Bis(pentafluorophenyl)bromonium cations with weak nucleophilic fluoroelementate anions

BrF3 reacts with MII(C6F5)2 (M = Zn, Cd, Hg) in organic solvents independent of the stoichiometry under formation of C6F5BrF2. Bromonium compounds [(C6F5)2Br]+ [EFn+l]- (E = Sb, As, B) are formed in equimolar reactions if additionally Lewis-acids EFn are present. [(C6F5)2Br]+ [BF4]- results in quantitative yield independent of the stoichiometry of substrates if BrF3 reacts with the Lewis-acidic aryl transfer reagent (C6F5)2BF. The molecular structure of the bromonium compounds [(C6F5)2Br]+ [BF4]- and [(C6F5)2Br]+ [AsF6]- can be interpreted in terms of two asymmetric hypervalent bonds at bromine(III). In solution the electrophilicity of Br(III) in [(C6F5)2Br]+ [EFn+l]- is responsible for the strong dependence of the 19F NMR shift values from the nucleophilicity of the solvent. Gauthier-Villars.