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Trimethyl-((E)-1-phenylsulfanyl-undeca-1,10-dienyloxy)-silane is a complex organic compound with the molecular formula C18H30OSi. It features a trimethylsilyl group (Si(CH3)3) attached to a long alkenyl chain with a phenylsulfanyl (C6H5S) group at the 1-position and a terminal alkene double bond at the 10-position. The compound exhibits an E-configuration, indicating that the phenylsulfanyl group and the terminal alkene double bond are on opposite sides of the molecule. This chemical is primarily used in organic synthesis as a protecting group for alcohols and as a reagent in various chemical reactions, particularly in the formation of carbon-sulfur bonds. Its unique structure and reactivity make it a valuable tool in the field of organic chemistry.

68117-67-9

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68117-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68117-67-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,1,1 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 68117-67:
(7*6)+(6*8)+(5*1)+(4*1)+(3*7)+(2*6)+(1*7)=139
139 % 10 = 9
So 68117-67-9 is a valid CAS Registry Number.

68117-67-9Downstream Products

68117-67-9Relevant academic research and scientific papers

Conversion of Carbon-Sulfur Linkages into Carbon-Silicon Ones via Reductive Silylation. Preparation of Silyl Enol Ethers of Acyltrimethylsilanes

Kuwajima, Isao,Mori, Akio,Kato, Masahiro

, p. 2634 - 2638 (2007/10/02)

Reductive cleavage of carbon-sulfur linkages of silyl enol ethers of thiocarboxylic S-esters can be induced by treatment with sodium or potassium-sodium alloy in the presence of chlorotrimethylsilane, and the corresponding silyl enol ethers of acyltrimethylsilanes can be prepared in high yields.

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