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Bis-dimethylamino-pentafluorphenyl-phosphin, also known as 2,4-bis(dimethylamino)-6-(pentafluorophenyl)phenylphosphine, is a phosphorus-containing organic compound with the molecular formula C14H14F5N2P. It is a colorless, crystalline solid that is soluble in common organic solvents. Bis-dimethylamino-pentafluorphenyl-phosphin is characterized by its pentafluorophenyl group and two dimethylamino groups attached to a phenyl ring, which contribute to its unique electronic properties and reactivity. It is often used as a ligand in coordination chemistry, particularly in the formation of transition metal complexes, due to its strong electron-donating ability and steric properties. The compound's stability and electronic properties make it a valuable building block in the synthesis of various organophosphorus compounds and catalysts.

5032-95-1

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5032-95-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5032-95-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,3 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5032-95:
(6*5)+(5*0)+(4*3)+(3*2)+(2*9)+(1*5)=71
71 % 10 = 1
So 5032-95-1 is a valid CAS Registry Number.

5032-95-1Relevant academic research and scientific papers

Synthesis and characterization of some perfluorophenylphosphine derivatives

Magnelli,Tesi,Lowe Jr.,Mcquistion

, p. 457 - 461 (2008/10/08)

Bis(pentafluorophenyl)chlorophosphine and pentafluorophenyldichlorophosphine are prepared in good yields from pentafluorophenylmagnesium bromide and phosphorus trichloride. The reactions of the halophosphines with the Lewis bases water, ammonia, dimethylamine, and 2-methylaziridine produced substituted phosphines. Oxidative chlorination of bis(pentafluorophenyl)phosphinamide followed by dehydrohalogenation gave perfluorophenylphosphonitriles. The infrared and pertinent proton magnetic resonance spectra of these compounds are discussed.

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