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1146729-41-0

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1146729-41-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1146729-41-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,6,7,2 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1146729-41:
(9*1)+(8*1)+(7*4)+(6*6)+(5*7)+(4*2)+(3*9)+(2*4)+(1*1)=160
160 % 10 = 0
So 1146729-41-0 is a valid CAS Registry Number.

1146729-41-0Downstream Products

1146729-41-0Relevant academic research and scientific papers

The enhanced asymmetric hydrogenation of unsymmetrical benzils to hydrobenzoin catalyzed by organosoluble zirconium phosphonate-immobilized ruthenium catalyst

Du, Yu,Feng, Dandan,Wan, Jingwei,Ma, Xuebing

, p. 49 - 58 (2014/06/09)

In this article, a successful design on translating a heterogeneous catalysis of chiral zirconium phosphonate-supported ruthenium catalyst into a homogeneous system was developed by the covalent attachment of chiral (R,R)-1,2-diphenyl-ethylenediamine [(R,R)-DPEN] into the backbone of zirconium phosphonate with the different arm lengths (n = 2, 4, 6) and immobilization of [RuCl2(p-cymene)]2. Their catalytic performances in the homogeneous asymmetric transfer hydrogenation of unsymmetrical benzils with m- and p-substituents were enhanced, and the excellent activities (>97.1% conv.), diastereomeric and enantiomeric purities (syn/anti = 11.0-29.4, 91.8-99.2%ee syn) were achieved. These homogeneous supported Ru catalysts could be quantitatively and readily recovered by addition of ethyl acetate and centrifugation by solid/liquid separation, and be reused for five times without significant loss of their catalytic performances with 97.0% conv.; 95.6% syn and syn/anti = 20.7.

Bidirectional metalation of hydrobenzoin: Direct access to new chiral ligands and auxiliaries

Cho, Inhee,Meimetis, Labros,Britton, Robert

supporting information; experimental part, p. 1903 - 1906 (2009/09/30)

A bidirectional ortho metalation of the readily available chiral diol hydrobenzoin has been developed that provides direct access to new ortho-functionalized hydrobenzoin derivatives. This one-pot procedure should broaden the utility of hydrobenzoin as an

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