34735-01-8 Usage
Uses
Used in Organic Synthesis:
Ethanone, 2,2'-(phenylphosphinylidene)bis[1-phenylis utilized as a reagent in organic synthesis, where it aids in the formation of new chemical bonds and the synthesis of complex organic molecules. Its unique structure and reactivity make it a valuable component in creating a wide range of organic compounds.
Used in Coordination Chemistry:
As a ligand in coordination chemistry, Ethanone, 2,2'-(phenylphosphinylidene)bis[1-phenylplays a crucial role in the formation of coordination compounds. It helps in the construction of metal complexes, which have applications in various fields such as catalysis, materials science, and medicinal chemistry. Ethanone, 2,2'-(phenylphosphinylidene)bis[1-phenyl-'s ability to bind with metal ions allows for the development of new catalysts and functional materials with improved properties.
Check Digit Verification of cas no
The CAS Registry Mumber 34735-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,7,3 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34735-01:
(7*3)+(6*4)+(5*7)+(4*3)+(3*5)+(2*0)+(1*1)=108
108 % 10 = 8
So 34735-01-8 is a valid CAS Registry Number.
34735-01-8Relevant academic research and scientific papers
Palladium(II)-catalyzed hydration of alkynylphosphonates to β-ketophosphonates
Li, Xiubin,Hu, Gaobo,Luo, Ping,Tang, Guo,Gao, Yuxing,Xu, Pengxiang,Zhao, Yufen
supporting information, p. 2427 - 2432 (2012/10/30)
A highly efficient palladium(II)-catalyzed hydration of a wide range of alkynylphosphonates to the corresponding β-ketophosphonates has been developed to give high yields at 80 °C in 1, 4-dioxane, with no acidic or alkaline cocatalysts required. The described catalytic system should provide an efficient alternative to highly toxic mercury-catalyzed methodologies and be useful in synthetic programs. Copyright
A synthetic approach to macrocyclic, chiral phosphane derivatives with crown-ether-like structures
Theil, Agnes,Hitce, Julien,Retailleau, Pascal,Marinetti, Angela
, p. 154 - 161 (2007/10/03)
(S,S)-Bis(2-hydroxypropyl)(phenyl)phosphane oxide has been prepared, either by ring-opening of (S)-propylene oxide with dilithio(phenyl)phosphane or by catalytic hydrogenation of bis(2-oxopropyl)(phenyl)phosphane oxide, promoted by ruthenium/MeO-BIPHEP. C
