217459-10-4 Usage
Uses
Used in Chemical Synthesis:
(S)-(-)-4-PYRROLIDINOPYRINDINYL(PENTAMETHYLCYCLOPENTADIENYL)IRON is used as a catalyst in the chemical synthesis industry for its ability to catalyze a range of chemical transformations. These include hydrogenation, cycloaddition, and carbon-carbon bond forming reactions, which are essential for the production of various chemicals and pharmaceuticals.
Used in Redox Reactions:
In the field of electrochemistry, (S)-(-)-4-PYRROLIDINOPYRINDINYL(PENTAMETHYLCYCLOPENTADIENYL)IRON is used as an electron transfer agent due to the potential provided by the iron center. This application is crucial for processes that involve redox reactions, such as energy storage and conversion systems.
Used in Catalyst Research and Development:
The unique reactivity and selectivity of (S)-(-)-4-PYRROLIDINOPYRINDINYL(PENTAMETHYLCYCLOPENTADIENYL)IRON make it a valuable compound for research and development in the field of catalysis. Scientists and researchers use (S)-(-)-4-PYRROLIDINOPYRINDINYL(PENTAMETHYLCYCLOPENTADIENYL)IRON to study and develop new catalysts with improved performance and efficiency for various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 217459-10-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,4,5 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 217459-10:
(8*2)+(7*1)+(6*7)+(5*4)+(4*5)+(3*9)+(2*1)+(1*0)=134
134 % 10 = 4
So 217459-10-4 is a valid CAS Registry Number.
217459-10-4Relevant academic research and scientific papers
Enantioselective synthesis of planar-chiral ferrocene-fused 4-pyridones and their application in construction of pyridine-based organocatalyst library
Ogasawara, Masamichi,Wada, Shiro,Isshiki, Erika,Kamimura, Takumi,Yanagisawa, Akira,Takahashi, Tamotsu,Yoshida, Kazuhiro
supporting information, p. 2286 - 2289 (2015/05/13)
A couple of planar-chiral ferrocene-fused 4-pyridone derivatives 2a and 2b were synthesized in enantiomerically pure form by scalable asymmetric transformations. Pyridones 2 are versatile precursors to various ferrocene-fused pyridine derivatives, which a