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1-Phenyl-1-(4-trimethylsiloxy)-phenylaethan, also known as 1-phenyl-1-(4-trimethylsiloxy)phenyl-2-phenylethane, is an organic compound with the molecular formula C21H26OSi. It is a colorless liquid that is soluble in organic solvents and has a molecular weight of 322.51 g/mol. 1-Phenyl-1-(4-trimethylsiloxy)-phenylaethan is characterized by the presence of a phenyl group, a trimethylsiloxy group, and an ethyl group, which contribute to its unique chemical properties. It is used in various chemical reactions and synthesis processes, particularly in the field of organic chemistry, due to its ability to act as a protecting group or a precursor in the formation of more complex molecules.

1029-77-2

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1029-77-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1029-77-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1029-77:
(6*1)+(5*0)+(4*2)+(3*9)+(2*7)+(1*7)=62
62 % 10 = 2
So 1029-77-2 is a valid CAS Registry Number.

1029-77-2Downstream Products

1029-77-2Relevant academic research and scientific papers

Organocatalytic asymmetric synthesis of 1,1-diarylethanes by transfer hydrogenation

Wang, Zhaobin,Ai, Fujin,Wang, Zheng,Zhao, Wanxiang,Zhu, Guangyu,Lin, Zhenyang,Sun, Jianwei

, p. 383 - 389 (2015/01/30)

A new organocatalytic transfer hydrogenation strategy for the asymmetric synthesis of 1,1-diarylethanes is described. Under mild conditions, a range of 1,1-diarylethanes substituted with an o-hydroxyphenyl or indole unit could be obtained with excellent efficiency and enantioselectivity. We also extended the protocol to an unprecedented asymmetric hydroarylation of 1,1-diarylalkenes with indoles for the synthesis of a range of highly enantioenriched 1,1,1-triarylethanes bearing acyclic all-carbon quaternary stereocenters. These diaryl- and triarylethanes exhibit impressive cytotoxicity against a number of human cancer cell lines. Preliminary mechanistic studies combined with DFT calculations provided important insight into the reaction mechanism.

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