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Tris(2,3-dimethylphenyl)phosphine is an organophosphorus compound with the chemical formula C21H21P. It is a colorless, crystalline solid that is soluble in organic solvents. tris(2,3-dimethylphenyl)phosphine is characterized by three 2,3-dimethylphenyl groups attached to a central phosphorus atom. It is used as a ligand in coordination chemistry, particularly in the formation of transition metal complexes, due to its ability to stabilize certain metal centers and influence the electronic properties of the resulting complexes. Tris(2,3-dimethylphenyl)phosphine is also employed as a reagent in various organic synthesis reactions, such as in the formation of phosphine oxides and as a reducing agent. Its stability and electronic properties make it a valuable tool in the field of chemistry.

29526-63-4

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29526-63-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29526-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,5,2 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29526-63:
(7*2)+(6*9)+(5*5)+(4*2)+(3*6)+(2*6)+(1*3)=134
134 % 10 = 4
So 29526-63-4 is a valid CAS Registry Number.

29526-63-4Downstream Products

29526-63-4Relevant academic research and scientific papers

Anodic Bahavior of Crowded Triarylphosphines. ESR Study of Triarylphosphoniumyl Radicals, Ar3P.+

Culcasi, Marcel,Berchadsky, Yves,Gronchi, Gerard,Tordo, Paul

, p. 3537 - 3542 (2007/10/02)

A large number of triarylphosphines exhibiting different steric hindrance has been prepared.The pyramidalization angle α of these compounds was calculated with use of the MM2 force field and was shown to depend almost exclusively on the number of ortho substituents on the phenyl rings.In a series of isosteric (same α) phosphines, the oxidation potential correlates with the sum of the ?+ Hammett parameters of the phenyl substituents.In the absence of oxygen, anodic oxidation of all the triarylphosphines bearing two o-methyl substituents on each phenyl ring is reversible and yields very persistent phosphoniumyl radicals.These radicals are easly detected by ESR in liquid solution and were shown to retain a pyramidal geometry that is significantly flattened compared to that of the parent phosphine.

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