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200192-50-3

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200192-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 200192-50-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,1,9 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 200192-50:
(8*2)+(7*0)+(6*0)+(5*1)+(4*9)+(3*2)+(2*5)+(1*0)=73
73 % 10 = 3
So 200192-50-3 is a valid CAS Registry Number.

200192-50-3Downstream Products

200192-50-3Relevant academic research and scientific papers

Towards long-living metathesis catalysts by tuning the N-heterocyclic carbene (NHC) ligand on trifluoroacetamide-activated boomerang ru complexes

Clavier, Herve,Caijo, Frederic,Borre, Etienne,Rix, Diane,Boeda, Fabien,Nolan, Steven P.,Mauduit, Marc

, p. 4254 - 4265 (2009)

The synthesis and characterization of three novel trifluoromethylamido- containing "boomerang" precatalysts bearing various N-heterocyclic carbene (NHC) ligands are reported. Comparative kinetic and stability studies show the significant effect of the NHC on the catalyst reaction profile. An investigation of the reaction scope for diverse metathesis transformations has allowed us to establish the influence of the NHC on catalyst activity, especially as a function of substrate steric bulk. The excellent stability of one of the novel precatalysts is disclosed, and allowed for its recovery at the end of catalytic reactions. Large-scale ring-closing metathesis, enyne-metathesis and cross-metathesis experiments have revealed the recoverability of the catalyst. ICP-MS analyses of the synthesized products reveal Ru contamination levels of less than 2.5 ppm.

Synthesis of oxygenated hererecycles from cyclic allylsiloxanes using ring-closing olefin metathesis

Meyer, Christophe,Cossy, Janine

, p. 7861 - 7864 (2007/10/03)

Cyclic allylsiloxanes were prepared from allyldimethylsilyl ethers of various alkenols by using a catalytic ring-closing metathesis (RCM) reaction. The transformation of these cyclic allylsiloxanes into stereoselectively substituted tetrahydrofurans and t

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