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(R)-3-(4-tert-butyldimethylsiloxylphenyl)-3-methylcyclohexanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1289577-11-2

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1289577-11-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1289577-11-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,9,5,7 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1289577-11:
(9*1)+(8*2)+(7*8)+(6*9)+(5*5)+(4*7)+(3*7)+(2*1)+(1*1)=212
212 % 10 = 2
So 1289577-11-2 is a valid CAS Registry Number.

1289577-11-2Downstream Products

1289577-11-2Relevant academic research and scientific papers

Synthesis of diverse β-quaternary ketones via palladium-catalyzed asymmetric conjugate addition of arylboronic acids to cyclic enones

Holder, Jeffrey C.,Goodman, Emmett D.,Kikushima, Kotaro,Gatti, Michele,Marziale, Alexander N.,Stoltz, Brian M.

, p. 5781 - 5792 (2015/08/03)

Abstract The development and optimization of a palladium-catalyzed asymmetric conjugate addition of arylboronic acids to cyclic enone conjugate acceptors is described. These reactions employ air-stable and readily-available reagents in an operationally si

Palladium-catalyzed asymmetric conjugate addition of arylboronic acids to five-, six-, and seven-membered β-substituted cyclic enones: enantioselective construction of all-carbon quaternary stereocenters

Kikushima, Kotaro,Holder, Jeffrey C.,Gatti, Michele,Stoltz, Brian M.

supporting information; experimental part, p. 6902 - 6905 (2011/06/19)

The first enantioselective Pd-catalyzed construction of all-carbon quaternary stereocenters via 1,4-addition of arylboronic acids to β-substituted cyclic enones is reported. Reaction of a wide range of arylboronic acids and cyclic enones using a catalyst

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