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o-<1-<(trimethylsilyl)oxy>vinyl>phenyl allyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69879-37-4

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69879-37-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69879-37-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,7 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69879-37:
(7*6)+(6*9)+(5*8)+(4*7)+(3*9)+(2*3)+(1*7)=204
204 % 10 = 4
So 69879-37-4 is a valid CAS Registry Number.

69879-37-4Relevant academic research and scientific papers

Highly regioselective synthesis of cyclic enol silyl ethers using ring-closing metathesis

Okada, Akihiro,Ohshima, Takashi,Shibasaki, Masakatsu

, p. 8023 - 8027 (2007/10/03)

We developed the first highly regioselective synthesis of cyclic enol ethers from readily accessible acyclic alkenyl ketones or acyclic alkenyl silyl esters using ring-closing metathesis (RCM). The RCM of acyclic enol silyl ethers was examined using Tebbe

Thermal addition reaction of aroylketene with 1-aryl-1- trimethylsilyloxyethylenes: Aromatic substituent effects of aroylketene and aryltrimethylsilyloxyethylene on their reactivity

Saitoh,Oyama,Sakurai,Niimura,Hinata,Horiguchi,Toda,Sano

, p. 956 - 966 (2007/10/03)

The thermal addition reaction of various aroylketenes (C) generated by the thermolysis of 5-aryldioxofurans (A) to 1-aryl-1-trimethylsilyloxyethylenes gave 1,5-diarylpentane-1,3,5-triones (D) and 2,6-diaryl-4H-pyran-4-ones (E). The introduction of electron withdrawing substituents in the aroylketene and of electron donating substituents facilitated the addition reaction. The observed substituent effects and the reaction mechanism are interpreted in terms of molecular orbital analyses.

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