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Phenylbis(trifluoromethyl)phosphine, also known as trifluoromethyldiphenylphosphine, is an organophosphorus compound with the chemical formula C8H5F6P. It is a colorless, volatile liquid that is sensitive to air and moisture. phenylbis(trifluoromethyl)phosphine is characterized by a phosphorus atom bonded to two trifluoromethyl groups and a phenyl group, which gives it unique chemical properties. It is used as a ligand in coordination chemistry, particularly in the synthesis of transition metal complexes, and as a reagent in organic synthesis due to its ability to stabilize certain intermediates. The compound is also of interest in materials science for its potential applications in the development of new materials with specific electronic properties.

1514-10-9

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1514-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1514-10-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1514-10:
(6*1)+(5*5)+(4*1)+(3*4)+(2*1)+(1*0)=49
49 % 10 = 9
So 1514-10-9 is a valid CAS Registry Number.

1514-10-9Relevant academic research and scientific papers

Cyanide initiated perfluoroorganylations with perfluoroorgano silicon compounds

Panne, Patricia,Naumann, Dieter,Hoge, Berthold

, p. 283 - 286 (2001)

Cyanophenylphosphanes, Ph2PCN or PhP(CN)2, do not react with Me3SiCF3 or Me3SiC6F5 in the absence of cyanide ions. Catalytic amounts of ionic cyanides such as [NEt4]CN

P-Stereogenic trifluoromethyl derivatives of josiphos: Synthesis, coordination properties, and applications in asymmetric catalysis

Buergler, Jonas F.,Niedermann, Katrin,Togni, Antonio

, p. 632 - 640 (2012/02/16)

Intermolecular nucleophilic substitution of a CF3 group of bis(trifluoromethyl)phosphanes by a lithiated Ugi's amine (4) affords both diastereoisomers of the corresponding P-stereogenic trifluoromethylphosphanes 6 and 7. Separation of the isomers by column chromatography on silica gel followed by substitution of the dimethylamino group with phosphanes or pyrazoles yields the bidentate P^P (9 and 10) or P^N ligands (12 and 13) without epimerization at the stereogenic phosphorus center. The coordination properties of these bidentate ligands were investigated on the basis of crystal structures of the corresponding palladium and rhodium complexes. IR spectroscopic measurements of rhodium-carbonyl complexes 16-23 indicated the strongly electronic-withdrawing character of these phosphanes. The catalytic potential of these ligands was demonstrated in the rhodium-catalyzed hydrogenation of olefins as well as in the palladium-catalyzed allylic alkylation reaction, where high activities and enantioselectivities were observed. CF3, more than just a simple substituent: Intra- and intermolecular nucleophilic substitutions of a CF 3 group in bis(trifluoromethyl)phosphanes were used in the preparation of bidentate ferrocenyl ligands bearing a P-stereogenic trifluoromethylphosphanyl group. High activities and enantioselectivities were achieved in rhodium-catalyzed olefin hydrogenation reactions and in palladium-catalyzed allylic alkylation reactions using these ligands. Copyright

The synthesis of tris(perfluoroalkyl)phosphines

Murphy-Jolly, Makeba B.,Lewis, Lesley C.,Caffyn, Andrew J. M.

, p. 4479 - 4480 (2007/10/03)

Tris(perfluoroalkyl)phosphines, of interest as turtable alternatives to the carbon monoxide ligand, can be synthesised by the nucleophile mediated reaction of perfluoroalkyltrimethylsilanes with triphenylphosphite; the method can be extended to diphosphines. The Royal Society of Chemistry 2005.

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