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Triphenylphosphin-α-dicyclohexylphosphino-aethyliden, also known as 1,1-bis(dicyclohexylphosphino)-2-phenyl-2-phosphinomethane, is a phosphorus-containing organometallic compound with the chemical formula C31H41P2. It is a white crystalline solid that is soluble in common organic solvents. Triphenylphosphin-α-dicyclohexylphosphino-aethyliden is a bidentate ligand, meaning it can form two separate bonds with a metal center, which makes it useful in various applications, including as a ligand in homogeneous catalysis. Its structure features a central carbon atom bonded to two dicyclohexylphosphino groups and a phenyl group, which contributes to its stability and reactivity in chemical reactions. The compound is synthesized through the reaction of triphenylphosphine with dicyclohexylphosphine and a suitable alkyl halide, and it is often used in the preparation of transition metal complexes that catalyze various industrially important reactions, such as hydrogenation and hydroformylation.

13411-70-6

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13411-70-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13411-70-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,1 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13411-70:
(7*1)+(6*3)+(5*4)+(4*1)+(3*1)+(2*7)+(1*0)=66
66 % 10 = 6
So 13411-70-6 is a valid CAS Registry Number.

13411-70-6Relevant academic research and scientific papers

Ylide-Functionalized Phosphines: Strong Donor Ligands for Homogeneous Catalysis

Scherpf, Thorsten,Schwarz, Christopher,Scharf, Lennart T.,Zur, Jana-Alina,Helbig, Andreas,Gessner, Viktoria H.

supporting information, p. 12859 - 12864 (2018/09/25)

Phosphines are important ligands in homogenous catalysis and have been crucial for many advances, such as in cross-coupling, hydrofunctionalization, or hydrogenation reactions. Herein we report the synthesis and application of a novel class of phosphines bearing ylide substituents. These phosphines are easily accessible via different synthetic routes from commercially available starting materials. Owing to the extra donation from the ylide group to the phosphorus center the ligands are unusually electron-rich and can thus function as strong electron donors. The donor capacity surpasses that of commonly used phosphines and carbenes and can easily be tuned by changing the substitution pattern at the ylidic carbon atom. The huge potential of ylide-functionalized phosphines in catalysis is demonstrated by their use in gold catalysis. Excellent performance at low catalyst loadings under mild reaction conditions is thus seen in different types of transformations.

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