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1134789-66-4

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1134789-66-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1134789-66-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,4,7,8 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1134789-66:
(9*1)+(8*1)+(7*3)+(6*4)+(5*7)+(4*8)+(3*9)+(2*6)+(1*6)=174
174 % 10 = 4
So 1134789-66-4 is a valid CAS Registry Number.

1134789-66-4Downstream Products

1134789-66-4Relevant articles and documents

Chiral undecagold clusters: Synthesis, characterization and investigation in catalysis

Andreiadis, Eugen S.,Vitale, Maxime R.,Mezailles, Nicolas,Le Goff, Xavier,Le Floch, Pascal,Toullec, Patrick Y.,Michelet, Veronique

, p. 10608 - 10616 (2011/01/05)

Enantiopure undecagold clusters protected by chiral atropisomeric diphosphine ligands (PP) have been synthesized by the stoichiometric reduction of the corresponding (PP)(AuCl)2 complexes with NaBH4. The molecular mono-disperse [Au11(PP)4Cl2]Cl species have been thoroughly characterized using an array of analytical techniques. 31P NMR experiments suggested the presence of a slow intramolecular ligand exchange process. Circular dichroism measurements showed that enantiomeric clusters display mirror-image chiroptical activity. Such undecagold clusters containing two chloride ligands bound to the peripheral Au(i) atoms were expected to display a carbophilic Lewis acidity similar to the well-documented molecular Au(i) complex catalysts. Chloride abstraction, performed to generate active Au+ sites, induced the Au11 cluster evolution to larger gold clusters and nanoparticles, together with Au(i) complexes, which, in fact, perform the catalysis. This result was corroborated by running an asymmetric tandem hydroarylation-carbocyclization reaction, for which the enantiomeric excesses obtained with Au11 clusters are similar to those reported using Au(i) complexes. The Royal Society of Chemistry 2010.

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