CAS 15596-07-3
:(Triphenylphosphoranylidene)ketene
Description:
Triphenylphosphoranylidene)ketene, with the CAS number 15596-07-3, is an organic compound characterized by the presence of a ketene functional group and a triphenylphosphoranylidene moiety. This compound typically exhibits a yellow to orange color and is known for its reactivity, particularly in forming various derivatives through nucleophilic addition reactions. The ketene part of the molecule contributes to its electrophilic nature, making it a useful intermediate in organic synthesis, especially in the formation of cyclic compounds and in reactions with nucleophiles. The presence of the triphenylphosphoranylidene group enhances its stability and solubility in organic solvents. Additionally, this compound may exhibit interesting optical properties and can participate in cycloaddition reactions. Its unique structure and reactivity profile make it a valuable compound in synthetic organic chemistry, particularly in the development of new materials and pharmaceuticals. As with many organophosphorus compounds, handling should be done with care due to potential toxicity and reactivity.
Formula:C20H15OP
InChI:InChI=1/C20H15OP/c21-16-17-22(18-10-4-1-5-11-18,19-12-6-2-7-13-19)20-14-8-3-9-15-20/h1-15H
SMILES:c1ccc(cc1)P(=C=C=O)(c1ccccc1)c1ccccc1
Synonyms:- Bestmann Ylide
- Ketenylidene(triphenyl)phosphorane
- (Triphenylphosphoranylidene)ethenone, Bestmann ylide, Ketenylidene(triphenyl)phosphorane
- (Triphenyl-Lambda~5~-Phosphanylidene)Ethenone
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Found 4 products.
(Triphenylphosphoranylidene)ketene
CAS:Formula:C20H15OPColor and Shape:White to Almost white powder to crystalMolecular weight:302.31Ethenone, 2-(triphenylphosphoranylidene)-
CAS:Formula:C20H15OPPurity:95%Color and Shape:SolidMolecular weight:302.3063(Triphenylphosphoranylidene)ketene
CAS:<p>(Triphenylphosphoranylidene)ketene</p>Purity:95%Molecular weight:302.31g/mol(Triphenylphosphoranylidene)ketene
CAS:<p>Triphenylphosphoranylidene)ketene is an amine-containing compound that is used as a catalyst in organic synthesis. It can be used in reactions involving the cleavage of carbon-carbon bonds and has been shown to oxidize alcohols, ethers, and esters. Triphenylphosphoranylidene)ketene was first synthesized in 1887 by the reaction of triphenylphosphine with ethylene dione.</p>Formula:C20H15OPPurity:Min. 95%Molecular weight:302.31 g/mol



