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1-(4-phenylphenyl)cyclopentan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

415898-26-9

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415898-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 415898-26-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,5,8,9 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 415898-26:
(8*4)+(7*1)+(6*5)+(5*8)+(4*9)+(3*8)+(2*2)+(1*6)=179
179 % 10 = 9
So 415898-26-9 is a valid CAS Registry Number.

415898-26-9Relevant academic research and scientific papers

Regio- and enantioselective Baeyer-Villiger oxidation: Kinetic resolution of racemic 2-substituted cyclopentanones

Zhou, Lin,Liu, Xiaohua,Ji, Jie,Zhang, Yuheng,Wu, Wangbin,Liu, Yangbin,Lin, Lili,Feng, Xiaoming

, p. 3938 - 3941 (2014)

A kinetic resolution of racemic 2-substituted cyclopentanones via highly regio- and enantioselective Baeyer-Villiger oxidation has been successfully developed. The reaction could afford the normal 6-substituted δ-lactones in up to 98% ee and >19/1 regioselectivity. Meanwhile, the unreacted ketones were recovered in excellent ee values (up to 98%). It represents the best results of the kinetic resolution of racemic 2-substituted cyclopentanones via nonenzymic asymmetric BV oxidation.

Terminal Trifluoromethylation of Ketones via Selective C-C Cleavage of Cycloalkanols Enabled by Hypervalent Iodine Reagents

Wu, Shuang,Li, Junzhao,He, Ru,Jia, Kunfang,Chen, Yiyun

supporting information, p. 9204 - 9209 (2021/11/30)

We report the first terminal trifluoromethylation at aryl and alkyl ketones' ?, or more remote sites via the selective C-C bond cleavage of cycloalkanols. The noncovalent interactions between alcohols and hypervalent iodines(III) reagents were disclosed to activate both alcohols and the Togni I reagent in the dual photoredox/copper catalysis for the transformation. This reaction was scalable to the gram-scale synthesis, applicable to the structurally complex steroid trifluoromethylation, and extendable to the pentafluoroethylation.

Catalytic Lactonization of Unactivated Aryl C-H Bonds with CO2: Experimental and Computational Investigation

Song, Lei,Zhu, Lei,Zhang, Zhen,Ye, Jian-Heng,Yan, Si-Shun,Han, Jie-Lian,Yin, Zhu-Bao,Lan, Yu,Yu, Da-Gang

supporting information, p. 3776 - 3779 (2018/07/21)

The first catalytic lactonization of unactivated aryl C-H bonds with CO2 to afford important phthalides is reported. Notably, this method features high selectivity, excellent functional group tolerance, smooth scalability, and facile product diversification. DFT calculations reveal that a novel insertion of two CO2 into the O-Pd bond of a palladacycle might be the key step, providing great potential and a different perspective for carbonylation with CO2.

Cyclopentyl sulfonamide derivatives

-

, (2008/06/13)

The present invention provides compounds of formula (I): useful for potentiating glutamate receptor function in a mammal and therefore, useful for treating a wide variety of conditions, such as psychiatric and neurological disorders.

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