5758-24-7

Basic information

• Product Name: bromotriphenylphosphonium bromide
• Synonyms: bromotriphenylphosphonium bromide
• CAS NO: 5758-24-7
• Molecular Weight: 422.099
• Mol File: 5758-24-7.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: bromotriphenylphosphonium bromide(CAS DataBase Reference)
• NIST Chemistry Reference: bromotriphenylphosphonium bromide(5758-24-7)
• EPA Substance Registry System: bromotriphenylphosphonium bromide(5758-24-7)

Safety Data

• Hazardous Substances Data: 5758-24-7(Hazardous Substances Data)

Upstream product

• 603-35-0 triphenylphosphine 

Downstream Products

• 54200-70-3 <3-Methyl-5-(2,3,6-trimethylphenyl)-cis-2-penten-4-in-1-yl>-triphenylphosphoniumbromid 
• 54200-91-8 3-methyl-5-(2,3,4-trimethylphenyl)penta-2,4-dien-1-yltriphenylphosphonium bromide 
• 54200-76-9 (2E,4EZ)-[3-methyl-5-(2,3,6-trimethylphenyl)-2,4-pentadienyl]triphenylphosphonium bromide 
• 54244-20-1 <2,7,11-Trimethyl-13-(2,3,6-trimethylphenyl)-2,4,6,8,10,12-tridecahexaen-1-yl>-triphenylphosphoniumbromid 
• 791-28-6 Triphenylphosphine oxide 
• 85924-42-1 [(3Z)-3-nonen-1-yl]triphenylphosphonium bromide 
• 900-92-5 triphenyl[(isopropyl)amino]phosphanium bromide 
• 1019841-41-8 4-methyl-2-(phenylethynyl)-(N-triphenylphosphoranylidene)phenylamine 
• 2526-64-9 dichlorotriphenylphosphorane 
• 603-35-0 triphenylphosphine 
• 81324-89-2 methoxytriphenylphosphonium trifluoromethanesulfonate 
• 101399-69-3 [Ph₃POSiMe₃](+)OTf(-) 
• 6395-93-3 anilinotriphenylphosphonium bromide 

Relevant articles and documents

Raman Spectra and Isomerism of Some Bromophenylphosphoranes PhnPBr(5-n) (1

A synthetic and Raman investigation of isomerism in the bromophenylphosphoranes has shown no evidence for ionic-covalent isomerism analogous to that in the chlorophenylphosphoranes.Two ionic modifications of PhPBr4 have been identified by Raman spectrosco

ACRYLAMI DE PHOTOI NI TI ATORS

Acrylamide photoinitiators are provided, in which a photoinitiator moiety and an acrylamide are incorporated into the photoinitiator structure.

Controlled formation of tetramethylammonium mono- and diylide

The reaction of tetramethylammonium bromide with n -butyllithium can selectively yield either trimethylammonium methylide or lithium dimethylammonium dimethylide, depending on the reaction conditions, as shown by 13C-NMR analysis of the deuterium-labelled species resulting from acidic trapping with DCl. So a simple synthesis of mono- or twice-functionalised methylammonium salts is allowed from a very usual starting material.