CAS 6228-47-3
:Propyltriphenylphosphonium bromide
Description:
Propyltriphenylphosphonium bromide is a quaternary ammonium salt characterized by its cationic structure, which consists of a triphenylphosphonium group attached to a propyl chain, along with a bromide anion. This compound typically appears as a white to off-white crystalline solid and is soluble in polar organic solvents, such as methanol and ethanol, but less soluble in non-polar solvents. It is known for its role as a phase transfer catalyst in organic synthesis, facilitating the transfer of reactants between immiscible phases. Additionally, it exhibits antimicrobial properties and has applications in various fields, including medicinal chemistry and materials science. The compound's stability and reactivity can be influenced by the nature of the substituents on the phosphonium ion, making it a versatile reagent in synthetic chemistry. Safety precautions should be taken when handling this compound, as it may pose health risks if ingested or inhaled.
Formula:C21H22P·Br
InChI:InChI=1S/C21H22P.BrH/c1-2-18-22(19-12-6-3-7-13-19,20-14-8-4-9-15-20)21-16-10-5-11-17-21;/h3-17H,2,18H2,1H3;1H/q+1;/p-1
InChI key:InChIKey=XMQSELBBYSAURN-UHFFFAOYSA-M
SMILES:[P+](CCC)(C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3.[Br-]
Synonyms:- (1-Propyl)triphenylphosphonium bromide
- Bromo(propyl)triphenylphosphorane
- N-Propyltriphenyl phosphonium Bromide
- NSC 50539
- Phosphonium, triphenylpropyl-, bromide
- Phosphonium, triphenylpropyl-, bromide (1:1)
- Propyl Triphenyl Phosphonium Bromide
- Propyl Triphenylphosphonium Bromide
- Triphenyl-n-propylphosphonium bromide
- Triphenylpropylphosphonium bromide
- n-Propyltriphenylphosphonium bromide
- See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 9 products.
Triphenylpropylphosphonium Bromide
CAS:Formula:C21H22BrPPurity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:385.28(1-Propyl)triphenylphosphonium bromide, 99%
CAS:<p>It is employed as a catalyst for the carboxylation of styrene oxide and as a reactant involved in epoxidation of arylalkenes, boration of allylic epoxides, Wittig reactions, selective dimerization of -olefins, and synthesis of indoles. It has also been shown to be part of Phosphonium salts, having a</p>Formula:C21H22BrPPurity:99%Color and Shape:White, Crystals or powder or crystalline powderMolecular weight:385.29Phosphonium, triphenylpropyl-, bromide
CAS:Formula:C21H22BrPPurity:95%Color and Shape:SolidMolecular weight:385.2771Propyl(triphenyl)phosphonium bromide
CAS:<p>Propyl(triphenyl)phosphonium bromide</p>Formula:C21H22P·BrPurity:99%Color and Shape: white. crystalline powderMolecular weight:385.28g/moln-Propyl-2,2,3,3,3-d5-triphenylphosphonium Bromide
CAS:Formula:CD3CD2CH2P(C6H5)3BrPurity:98 atom % DColor and Shape:White SolidMolecular weight:389.09563Propyltriphenylphosphonium bromide
CAS:Formula:C21H22BrPPurity:95%Color and Shape:SolidMolecular weight:385.285n-Propyltriphenylphosphonium Bromide
CAS:Controlled Product<p>Stability Hygroscopic<br>Applications n-Propyltriphenylphosphonium Bromide, is an analogue of phosphonium, acting as reversible inhibitors of cholinesterases of different animals. It has also been shown to be part of Phosphonium salts, having antiviral activity against influenza virus A.<br>References Basova, N. E., et al.: oklady Biochem. Biophys., 434, 245 (2010); Romanov, G. V., et al.: Khimiko-Farmatsevticheskii Zhurnal, 24, 28 (1990);<br></p>Formula:C21H22BrPColor and Shape:NeatMolecular weight:385.28(1-Propyl)triphenylphosphonium bromide
CAS:<p>(1-Propyl)triphenylphosphonium bromide is an organic chemical compound. It is a colorless solid that is soluble in organic solvents such as chloroform and ether, but insoluble in water. The chemical structure of (1-propyl)triphenylphosphonium bromide was determined by NMR spectra and chemical ionization mass spectroscopy. The viscosity of the liquid at room temperature is 0.5 Pa·s. Reaction intermediates have been detected by GC/MS analysis, which includes protonated 1-propyl triphenylphosphonium cation, phosphonium ylide, and phosphonium carbenoid. This product has shown inhibitory effects on the reaction between aldehyde groups and fatty acid chains in the presence of potassium hydroxide or sodium hydroxide solutions.</p>Purity:Min. 95%









