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2-(tert-butyldimethylsilyl)-2-(4-methoxyphenyl)-1,3-dithiane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1269230-75-2

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1269230-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1269230-75-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,9,2,3 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1269230-75:
(9*1)+(8*2)+(7*6)+(6*9)+(5*2)+(4*3)+(3*0)+(2*7)+(1*5)=162
162 % 10 = 2
So 1269230-75-2 is a valid CAS Registry Number.

1269230-75-2Downstream Products

1269230-75-2Relevant academic research and scientific papers

Synthesis of Chiral α-Aminosilanes through Palladium-Catalyzed Asymmetric Hydrogenation of Silylimines

Fan, Dongyang,Liu, Yang,Jia, Jia,Zhang, Zhenfeng,Liu, Yangang,Zhang, Wanbin

, p. 1042 - 1045 (2019/05/16)

The asymmetric hydrogenation of silylimines was first developed by using a palladium complex of a P-stereogenic diphosphine ligand as the catalyst, affording the valuable chiral α-aminosilanes with quantitative conversions and excellent enantioselectiviti

Enantio-, Regio- and Chemoselective Copper-Catalyzed 1,2-Hydroborylation of Acylsilanes

Nagy, Audric,Collard, Laurent,Indukuri, Kiran,Leyssens, Tom,Riant, Olivier

, p. 8705 - 8708 (2019/06/13)

Enantioselective synthesis of synthetically significant (α-hydroxyallyl)silanes, (α-hydroxyaryl)silanes, and (α-hydroxyalkyl)silanes is reported. The present copper-catalyzed 1,2-selective hydroborylation of acylsilanes affords the aforementioned products

Oxidative [1,2]-Brook Rearrangements Exploiting Single-Electron Transfer: Photoredox-Catalyzed Alkylations and Arylations

Deng, Yifan,Liu, Qi,Smith, Amos B.

, p. 9487 - 9490 (2017/07/24)

Oxidative [1,2]-Brook rearrangements via hypervalent silicon intermediates induced by photoredox-catalyzed single-electron transfer have been achieved, permitting the formation of reactive radical species that can engage in alkylations and arylations.

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