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Cycloheptanone, 2-hydroxy-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

98017-34-6

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98017-34-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98017-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,0,1 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 98017-34:
(7*9)+(6*8)+(5*0)+(4*1)+(3*7)+(2*3)+(1*4)=146
146 % 10 = 6
So 98017-34-6 is a valid CAS Registry Number.

98017-34-6Relevant academic research and scientific papers

Bronsted Acid Mediated Direct α-Hydroxylation of Cyclic α-Branched Ketones

Shevchenko, Grigory A.,Dehn, Stefanie,List, Benjamin

supporting information, p. 2298 - 2300 (2018/10/20)

We report a Bronsted acid mediated direct α-hydroxylation of cyclic α-branched ketones via a tandem aminoxylation/N-O bond-cleavage process. Nitrosobenzene is used as the oxidant and subsequently promotes the liberation of the free alcohol. The desired pr

Iron(iii) chloride hexahydrate-promoted selective hydroxylation and chlorination of benzyl ketone derivatives for the construction of hetero-quaternary scaffolds

Chen, Tao,Peng, Rui,Hu, Wenxin,Zhang, Fu-Min

supporting information, p. 9859 - 9867 (2016/10/31)

A novel and tunable α-hydroxylation/α-chlorination of benzyl ketone derivatives has been developed for the construction of hetero-quaternary carbon centers by iron(iii) chloride hexahydrate mediated selective transformations through the application of dif

Electroreductive acylation of aromatic ketones with acylimidazoles

Kise, Naoki,Agui, Syun,Morimoto, Shinji,Ueda, Nasuo

, p. 9407 - 9410 (2007/10/03)

The intermolecular reductive coupling of aromatic ketones with acylimidazoles was effected by electroreduction in the presence of chlorotrimethylsilane and gave α-trimethylsiloxy ketones and esters. The best result was obtained using Bu4NPF6 as a supporting electrolyte and a Pb cathode in THF. The α-trimethylsiloxy-containing products were transformed to the corresponding α-hydroxy ketones and esters by treatment with TBAF in THF. This method was also effective for the intramolecular reductive coupling of δ- and ε-keto acylimidazoles.

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