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Ethenamine, 2-(diphenylphosphinyl)-N,N-dimethyl-, also known as (dimethylamino)(2-diphenylphosphinoethyl)amine or DMPEA, is an organophosphorus compound with the chemical formula C16H18NP. It is a colorless to pale yellow liquid with a molecular weight of 259.29 g/mol. DMPEA is a chelating agent and a ligand used in various applications, including the synthesis of metal complexes and as a reagent in organic chemistry. It is soluble in common organic solvents and has a melting point of -40°C. Due to its phosphorus and nitrogen donor atoms, DMPEA can form stable complexes with transition metals, making it a valuable compound in coordination chemistry and catalysis.

5773-12-6

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5773-12-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5773-12-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,7 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5773-12:
(6*5)+(5*7)+(4*7)+(3*3)+(2*1)+(1*2)=106
106 % 10 = 6
So 5773-12-6 is a valid CAS Registry Number.

5773-12-6Downstream Products

5773-12-6Relevant academic research and scientific papers

Reactions with Phosphine Alkylenes, XLV. Reactions of Alkylidenetriphenylphosphoranes with Tetramethylformamidinium Chloride. Synthesis of triphenylphosphonium Chloride and (Formylalkylidene)triphenylphosphoranes

Bestmann, Hans Juergen,Schmid, Guenter,Oechsner, Helmut,Ermann, Peter

, p. 1561 - 1571 (2007/10/02)

Phosphonium ylides 1 react with tetramethylformamidinium chloride (2) to form enamine phosphonium chlorides 8 and the formic orthoamide 7.The salts 8 show temperature depending 1H NMR spectra with respect to the protons of the dimethylamino group (hindered rotation around the C - N(CH3)2 bond).Treatment of 8 with acids and subsequently with bases gives rise to the formation of the formyl ylides 19. 8a is deprotonated with sodium amide to give the phosphaallene ylide 20, which reacts with water to yield the phosphane oxide 21, and with methyl iodide stereospecifically to form 8b.

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