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α-(Trimethylsiloxy)-m-fluorstyrol is a complex organic compound characterized by its unique molecular structure. It features a fluorostyrene backbone, which is a derivative of styrene with a fluorine atom replacing one of the hydrogen atoms on the phenyl ring. The α-position of this fluorostyrene is substituted with a trimethylsiloxy group, which consists of a silicon atom bonded to three methyl groups and an oxygen atom. α-(Trimethylsiloxy)-m-fluorstyrol is of interest in organic synthesis and materials science due to its potential applications in the creation of new polymers and other advanced materials. Its specific properties, such as reactivity and stability, make it a valuable component in the development of novel chemical compounds and technologies.

52186-49-9

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52186-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52186-49-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,1,8 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 52186-49:
(7*5)+(6*2)+(5*1)+(4*8)+(3*6)+(2*4)+(1*9)=119
119 % 10 = 9
So 52186-49-9 is a valid CAS Registry Number.

52186-49-9Relevant academic research and scientific papers

Photoredox-Catalyzed Decarboxylative Alkylation of Silyl Enol Ethers to Synthesize Functionalized Aryl Alkyl Ketones

Kong, Weiguang,Yu, Changjiang,An, Hejun,Song, Qiuling

, p. 349 - 352 (2018)

Photoredox-catalyzed decarboxylative alkylation of silyl enol ethers has been developed. Diverse functionalized aryl alkyl ketones were afforded in modest to good yields using N-(acyloxy)phthalimide as an easy access alkyl radical source under mild and operationally simple conditions. The excellent performance of drug molecules such as fenbufen and indomethacin and naturally occurring carboxylic acids such as stearic acid and dehydrocholic acid further demonstrated the practicability of the reaction.

Palladium-Catalyzed [5 + 2] Annulation of Vinylethylene Carbonates with Barbiturate-Derived Alkenes

Chen, Yuehua,Deng, Hao,Gao, Xing,Guo, Hongchao,Jiang, Feng,Wang, Wei,Wu, Yongjun,Zhu, Dongyu

supporting information, p. 7158 - 7163 (2020/10/02)

A palladium/XantPhos-catalyzed [5 + 2] annulation of VECs with electron-deficient alkenes having an isolated carbon-carbon double bond has been developed to afford spirobarbiturate-tetrahydrooxepines. This study provides an expedient assembly of biologically interesting spirobarbiturate-tetrahydrooxepines. The easy scalability and versatile transformability of the reaction products were also exhibited.

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