877676-52-3 Usage
Uses
Used in Pharmaceutical Industry:
(dithiodiphenylphosphinate)(phenyl)(triphenylphosphine)palladium(II) is used as a catalyst for the synthesis of various pharmaceutical compounds. Its ability to facilitate cross-coupling reactions and carbon-carbon bond formation is crucial in the production of complex organic molecules with potential therapeutic applications.
Used in Chemical Synthesis:
In the chemical synthesis industry, (dithiodiphenylphosphinate)(phenyl)(triphenylphosphine)palladium(II) serves as a versatile catalyst for a wide range of organic reactions. Its complex structure allows it to promote the formation of carbon-carbon bonds and other critical bond types, enabling the synthesis of diverse organic compounds with various applications.
Used in Material Science:
(dithiodiphenylphosphinate)(phenyl)(triphenylphosphine)palladium(II) is employed as a catalyst in the development of new materials with specific properties. Its role in facilitating cross-coupling reactions and carbon-carbon bond formation is essential in creating materials with tailored characteristics for various applications, such as electronics, energy storage, and advanced coatings.
Used in Research and Development:
In academic and industrial research settings, (dithiodiphenylphosphinate)(phenyl)(triphenylphosphine)palladium(II) is utilized as a catalyst to explore new reaction pathways and develop innovative synthetic methods. Its unique properties make it an invaluable tool for advancing the understanding of organic chemistry and discovering new compounds with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 877676-52-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,7,6,7 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 877676-52:
(8*8)+(7*7)+(6*7)+(5*6)+(4*7)+(3*6)+(2*5)+(1*2)=243
243 % 10 = 3
So 877676-52-3 is a valid CAS Registry Number.
877676-52-3Relevant academic research and scientific papers
Esterhuysen, Catharine,Kruger, Gert J.,Blewett, Gavin,Raubenheimer, Helgard G.
, p. 609 - 616 (2006)
Two crystalline forms of (dithiodiphenylphosphinate)(phenyl) (triphenylphosphine)-palladium(II) (C36H30P 2PdS2), one without solvent, the other containing THF (C4H8O), are obtained after reaction of sodium diphenyldithiophosphinate with (phenyl) (bis-triphenylphosphine) palladium(II) chloride and crystallisation from two different solvent mixtures. The molecular structures, as determined by single crystal X-ray diffraction, differ in the planarity of the 4-membered palladium dithiophosphinate rings. The experimental conformations have been compared to the conformations of four-membered metal-S2P rings reported in the Cambridge Structural Database. A flat conformation is more common than a puckered one. DFT calculations at the B3LYP level of theory indicate that the flat conformation of a model metallodithiophosphinate ring is very slightly lower in energy (1.2 kcal/mol) than the puckered conformation.
