CAS 5044-52-0
:Phosphonium, ethenyltriphenyl-, bromide (1:1)
Description:
Phosphonium, ethenyltriphenyl-, bromide (1:1), commonly referred to as a phosphonium salt, is characterized by its quaternary ammonium structure where a phosphorus atom is bonded to three phenyl groups and one ethenyl group, along with a bromide counterion. This compound typically exhibits properties associated with ionic salts, such as high solubility in polar solvents and the ability to conduct electricity in solution. The presence of the ethenyl group introduces potential for reactivity, particularly in polymerization reactions or as a ligand in coordination chemistry. Phosphonium salts are often used in organic synthesis, catalysis, and as intermediates in the preparation of various organic compounds. The stability of the phosphonium ion can vary depending on the substituents attached to the phosphorus atom, influencing its reactivity and applications. Additionally, the bromide ion can participate in nucleophilic substitution reactions, making this compound versatile in synthetic organic chemistry. Overall, phosphonium, ethenyltriphenyl-, bromide is a significant compound in both academic and industrial chemistry contexts.
Formula:C20H18BrP
InChI:InChI=1/C20H18P.BrH/c1-2-21(18-12-6-3-7-13-18,19-14-8-4-9-15-19)20-16-10-5-11-17-20;/h2-17H,1H2;1H/q+1;/p-1
InChI key:InChIKey=VRAYVWUMBAJVGH-UHFFFAOYSA-M
SMILES:[P+](C=C)(C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3.[Br-]
Synonyms:- Bromotriphenylvinylphosphorane
- Ethenyl(Triphenyl)Phosphonium Bromide
- NSC 84065
- Phosphonium, ethenyltriphenyl-, bromide
- Phosphonium, ethenyltriphenyl-, bromide (1:1)
- Phosphonium, triphenylvinyl-, bromide
- Schweizers
- Triphenylvinylphosphonium bromide
- Vinyl(triphenyl)phosphine bromide
- Vinyltriphenylphosphonium bromide
- SCHWEIZER'S REAGENT
- VINYL TRIPHENYLPHOSPHONIUM BROMIDE (TRIPHENYL VINYLPHOSPHONIUM BROMIDE)
- Schweizers Reagent, Vinyltriphenylphosphonium bromide
- Vinyltriphenylphosphoniumbromide,97%
- Schweizer'sReagent~Triphenylvinylphosphoniumbromide
- See more synonyms
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Found 6 products.
Vinyltriphenylphosphonium bromide, 97%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C20H18BrPPurity:97%Color and Shape:White to cream or pale yellow, PowderMolecular weight:369.24Triphenyl(vinyl)phosphonium bromide
CAS:Formula:C20H18BrPPurity:97%Color and Shape:SolidMolecular weight:369.2347Triphenyl(Vinyl)Phosphonium Bromide
CAS:Triphenyl(Vinyl)Phosphonium BromidePurity:97%Molecular weight:369.23g/molTriphenyl(vinyl)phosphonium Bromide
CAS:Formula:C20H18BrPPurity:>96.0%(T)(HPLC)Color and Shape:White to Orange to Green powder to crystalMolecular weight:369.24Triphenyl(vinyl)phosphonium bromide
CAS:Formula:C20H18BrPPurity:97%;RGColor and Shape:Liquid, No data available.Molecular weight:369.242Triphenylvinylphosphonium Bromide
CAS:<p>Triphenylvinylphosphonium bromide is a model system that is used to study the reaction mechanism of hydroxyl group and hydrogen fluoride. It can be used to synthesize heterocycles such as quinolines. Triphenylvinylphosphonium bromide is also used in the synthesis of sodium salts, which are commonly used in the laboratory. This compound has been shown to have an effect on protein synthesis and crystalline cellulose, which is a carbohydrate polymer that can be hydrolyzed by enzymes. Triphenylvinylphosphonium bromide reacts with carbonyl groups and metal hydroxides, leading to biochemical properties such as carboxy groups and dimethyl fumarate. Triphenylvinylphosphonium bromide also inhibits non-nucleoside inhibitors, specifically 2',3'-dideoxyinosine (ddI).</p>Formula:C20H18BrPPurity:Min. 95%Molecular weight:369.23 g/mol





