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(4-methoxyphenyl)methyl(1-naphthyl)phenylsilane is a complex organic compound with the molecular formula C25H22O2Si. It is a derivative of phenylsilane, characterized by the presence of a silicon atom bonded to a phenyl group, a 1-naphthyl group, and a 4-methoxyphenyl group. The 4-methoxyphenyl group introduces an ether linkage, which can influence the compound's reactivity and solubility. (4-methoxyphenyl)methyl(1-naphthyl)phenylsilane is of interest in organic synthesis, particularly in the formation of silicon-containing molecules, which can be used in various applications such as pharmaceuticals, materials science, and as intermediates in the synthesis of more complex molecules. Its structure provides a unique combination of aromatic and heteroatom functionality, which can lead to interesting chemical properties and reactivity patterns.

978-90-5

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978-90-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 978-90-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,7 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 978-90:
(5*9)+(4*7)+(3*8)+(2*9)+(1*0)=115
115 % 10 = 5
So 978-90-5 is a valid CAS Registry Number.

978-90-5Downstream Products

978-90-5Relevant academic research and scientific papers

Copper-catalyzed arylation of chlorosilanes with grignard reagents

Morita, Eiji,Murakami, Kei,Iwasaki, Masayuki,Hirano, Koji,Yorimitsu, Hideki,Oshima, Koichiro

scheme or table, p. 1012 - 1014 (2011/02/26)

Nucleophilic substitution reactions of chlorosilanes with aryl Grignard reagents take place efficiently in the presence of copper(I) iodide to afford tetraorganosilanes.

Silver-catalyzed transmetalation between chlorosilanes and aryl and alkenyl Grignard reagents for the synthesis of tetraorganosilanes

Murakami, Kei,Hirano, Koji,Yorimitsu, Hideki,Oshima, Koichiro

supporting information; scheme or table, p. 5833 - 5835 (2009/03/11)

(Chemical Equation Presented) The silver savior: Nucleophilic substitution reactions of chlorosilanes with aryl Grignard reagents have been developed which take place under silver catalysis to afford tetraorganosilanes (see scheme). This transformation is likely to be promoted by diarylargentate reagents that are generated in situ.

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