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(E)-1-methoxy-2-phenyl-1-trimethylsilylethene is an organic compound characterized by its unique structure, which features a vinyl group (C=C) with a trimethylsilyl group (SiMe3) attached to one carbon and a phenyl group (C6H5) attached to the other carbon. The molecule also contains a methoxy group (OCH3) bonded to the carbon adjacent to the trimethylsilyl group. (E)-1-methoxy-2-phenyl-1-trimethylsilylethene is known for its stability and reactivity, which can be attributed to the presence of the electron-donating trimethylsilyl group and the electron-withdrawing phenyl group. It is often used in organic synthesis as a precursor for the preparation of various functionalized olefins and as a protecting group in the synthesis of complex organic molecules. The compound's properties, such as its stability towards hydrolysis and its ability to participate in various chemical reactions, make it a valuable tool in the field of organic chemistry.

73451-95-3

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73451-95-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73451-95-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,4,5 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 73451-95:
(7*7)+(6*3)+(5*4)+(4*5)+(3*1)+(2*9)+(1*5)=133
133 % 10 = 3
So 73451-95-3 is a valid CAS Registry Number.

73451-95-3Relevant academic research and scientific papers

Unsaturated Acyl Derivatives of Silicon, Germanium, and Tin from Metalated Enol Ethers

Soderquist, John A.,Hassner, Alfred

, p. 1577 - 1583 (2007/10/02)

The preparation of 1-lithio derivatives of some conjugated vinyl ethers is described.Reaction of these compounds with the chlorotrimethyl derivatives of silicon, germanium, and tin gives the corresponding metallovinyl ethers in 50-80percent yield.At least in the case of silicon these reactions proceed with retention of stereochemistry.The silyl compounds undergo Z E photoisomerization.Hydrolysis of the ethers in aqueous acetone gives the corresponding acylmetallanes in 60-75percent yield.The metalation and hydrolysis reactions are examined in some detail.The spectral properties of these novel unsaturated acylmetallanes are presented and discussed.

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