866825-79-8 Usage
Uses
Used in Organic Synthesis:
Palladium, chloro[2-[1-[(4-methylphenyl)imino-.kappa.N]ethyl]ferrocenyl-.kappa.C](tricyclohexylphosphine)is used as a catalyst in organic synthesis for its ability to facilitate various organic transformations. Its unique catalytic properties make it suitable for promoting reactions that involve the formation of carbon-carbon and carbon-heteroatom bonds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Palladium, chloro[2-[1-[(4-methylphenyl)imino-.kappa.N]ethyl]ferrocenyl-.kappa.C](tricyclohexylphosphine)is used as a catalyst for the synthesis of fine chemicals and pharmaceuticals. Its stability and reactivity contribute to the efficient production of complex organic molecules required for the development of new drugs and therapeutic agents.
Used in Cross-Coupling Reactions:
Palladium, chloro[2-[1-[(4-methylphenyl)imino-.kappa.N]ethyl]ferrocenyl-.kappa.C](tricyclohexylphosphine)is also utilized in cross-coupling reactions, a type of chemical reaction that combines two organic molecules to form a new compound. Its catalytic properties make it an important component in the synthesis of various organic compounds, including those used in the production of specialty chemicals and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 866825-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,8,2 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 866825-79:
(8*8)+(7*6)+(6*6)+(5*8)+(4*2)+(3*5)+(2*7)+(1*9)=228
228 % 10 = 8
So 866825-79-8 is a valid CAS Registry Number.
866825-79-8Relevant academic research and scientific papers
Gong, Junfang,Liu, Guangyu,Du, Chenxia,Zhu, Yu,Wu, Yangjie
, p. 3963 - 3969 (2005)
The air and moisture stable tricyclohexylphosphine (PCy3) adducts of dimeric cyclopalladated ferrocenylimines 5 and 6 have been easily synthesized and successfully used in palladium-catalyzed Suzuki cross-coupling of aryl chlorides. Using 0.1 mol% of 6 in the presence of 2 equivalent of Cs2CO3 as base in dioxane at 100 °C provided coupled products in excellent yields in the reaction of non-activated and deactivated aryl chlorides with phenylboronic acid. For activated chlorides such as 4-chloronitrobenzene and 4-chloroacetophenone, the catalyst loadings could be lowered to 0.01 mol% without loss of activity.
