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1'-phenyl-<1'-oxy>-2'-<<(1,1-dimethylethyl)dimethylsilyl>-oxy>ethane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

166248-63-1

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166248-63-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 166248-63-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,2,4 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 166248-63:
(8*1)+(7*6)+(6*6)+(5*2)+(4*4)+(3*8)+(2*6)+(1*3)=151
151 % 10 = 1
So 166248-63-1 is a valid CAS Registry Number.

166248-63-1Relevant academic research and scientific papers

PYRIMIDONE DERIVATIVES USED AS TAU PROTEIN KINASE 1 INHIBITORS

-

, (2011/02/24)

A compound represented by the formula (I) or a pharmaceutically acceptable salt thereof: wherein Z represents nitrogen atom or C-X; X represents hydrogen atom or fluorine atom; R1 is hydrogen atom or a C1 -C3 alkyl group; L represents single bond or a C1 -C6 alkylene group which may be substituted; Y represents single bond, sulfur atom, oxygen atom, NH, or the like; R2 represents hydrogen atom or a cyclic group which may be substituted, which is used for preventive and/or therapeutic treatment of a disease caused by abnormal activity of tau protein kinase 1 such as a neurodegenerative diseases (e.g. Alzheimer disease).

Acid-catalyzed solvolysis of polyenol ethers. III. Effect of the alkoxy moiety

Nieuwenhuis, Saskia A. M.,Vertegaal, Louis B. J.,De Zoete, Marian C.,Van Der Gen, Arne

, p. 13207 - 13230 (2007/10/02)

The dependence of the solvolysis of polyenol ethers on the nature of the alkoxy moiety has been studied. A new reaction path, leading to the formation of ω-hydroxy (methoxy) substituted aldehydes and -esters, was established. The proposed reaction pathway (scheme 6) is initiated by an electron transfer from the polyenol ether to molecular oxygen, followed by combination of the two radicals to a peroxide zwitterion. Upon protonation, solvent adds to the ω-carbon atom of the polyene to give an intermediate that can either loose water to form an ester, or loose the alkoxy moiety to give an aldehyde. This mechanism is believed to be involved in the strong mutagenic activity displayed by many polyenol ethers, including the natural mutagen fecapentaene-12.

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