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(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-((R)-6-methylheptan-2-yl)-3-phenoxy-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13913-60-5

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13913-60-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13913-60-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,1 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13913-60:
(7*1)+(6*3)+(5*9)+(4*1)+(3*3)+(2*6)+(1*0)=95
95 % 10 = 5
So 13913-60-5 is a valid CAS Registry Number.

13913-60-5Downstream Products

13913-60-5Relevant academic research and scientific papers

Montmorillonite Clay Catalysis. Part 13.1 Etherification of Cholesterol Catalysed by Montmorillonite K-10

Lu, Bo,Li, Li-Jun,Li, Tong-Shuang,Li, Ji-Tai

, p. 604 - 605 (1998)

The preparation of cholesteryl ethers from alcohols and phenols with cholesterol is carried out at 50-70 °C by using montmorillonite K-10 as an acid catalyst in chloroform or cyclohexane.

Radical Anion Promoted Chemoselective Cleavage of Csp2-S Bond Enables Formal Cross-Coupling of Aryl Methyl Sulfones with Alcohols

Bai, Jixiang,Wang, Tianxin,Dai, Botao,Liu, Qingchao,Yu, Peiyuan,Jia, Tiezheng

supporting information, p. 5761 - 5765 (2021/08/16)

A novel formal cross-coupling of aryl methyl sulfones and alcohols affording alkyl aryl ethers via an SRN1 pathway is developed. Two marketed antitubercular drugs were efficiently prepared employing this approach as the key step. A dimsyl-anion initiated radical chain process was revealed as the major pathway. DFT calculations indicate that the formation of a radical anion via nucleophilic addition of alkoxide to the aryl radical is the key step in determining the observed chemoselectivity.

Metal-Free I2-Catalyzed Highly Selective Dehydrogenative Coupling of Alcohols and Cyclohexenones

Liang, Yu-Feng,Yuan, Yizhi,Shen, Tao,Song, Song,Jiao, Ning

, p. 233 - 240 (2018/02/19)

The I2 catalyzed highly selective oxidative condensation of cyclohexenones and alcohols for the synthesis of aryl alkyl ethers has been described. DMSO is employed as the mild terminal oxidant. This novel methodology offers a metal-free reaction condition, operational simplicity and broad substrate scope to afford valuable products from inexpensive reagents. Various meta-substituted aromatic ethers which are hardly synthesized from the reported methods requiring meta-substituted phenols, are efficiently prepared by the present protocol.

3α,5α-Cyclocholestan-6β-yl ethers as donors of the holesterol moiety for the electrochemical synthesis f cholesterol glycoconjugates

Tomkiel, Aneta M.,Biedrzycki, Adam,Ploszyska, Jolanta,Narg, Dorota,Sobkowiak, Andrzej,Morzycki, Jacek W.

, p. 162 - 168 (2015/02/05)

3α,5α-Cyclocholestan-6β-yl alkyl and aryl ethers were proved to be efficient cholesteryl donors in the electrochemical synthesis of glycoconjugates. 3α,5α-Cyclocholestan-6β-ol (i-cholesterol) and its tert-butyldimethylsilyl ether can also be used for this

Catalytic aerobic synthesis of aromatic ethers from non-aromatic precursors

Simon, Marc-Olivier,Girard, Simon A.,Li, Chao-Jun

supporting information; experimental part, p. 7537 - 7540 (2012/09/10)

Only little waste: Aryl ether formation is accomplished by oxidative condensation of alcohols and 2-cyclohexenones. The reaction complements the existing methods used by synthetic chemists to obtain aryl ethers, and allows a straightforward access to a wide range of functionalized products. In addition, the catalytic reaction with O2 as the oxidant generates water as the only by-product and provides a greener approach to aryl ethers. Copyright

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