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Trimethyl-((1E,4E)-4-phenylsulfanyl-nona-1,4-dienyloxy)-silane is a complex organic compound with the molecular formula C18H30O2SSi. It is characterized by a unique structure that includes a trimethylsilyl group, a phenylsulfanyl group, and a nona-1,4-dienyloxy chain. The compound is notable for its specific arrangement of double bonds (1E,4E) in the nona-1,4-dienyloxy moiety, which contributes to its chemical reactivity and potential applications in organic synthesis. Trimethyl-((1E,4E)-4-phenylsulfanyl-nona-1,4-dienyloxy)-silane may be used as a reagent in the formation of various organic molecules, particularly those requiring a sulfur-phenyl linkage, and could be involved in reactions that benefit from the steric and electronic properties conferred by the trimethylsilyl group.

80399-05-9

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80399-05-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80399-05-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,3,9 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 80399-05:
(7*8)+(6*0)+(5*3)+(4*9)+(3*9)+(2*0)+(1*5)=139
139 % 10 = 9
So 80399-05-9 is a valid CAS Registry Number.

80399-05-9Relevant academic research and scientific papers

Bifunctional Cyclopropyl Reagents: Stereocontrolled Approach to Vinyl Sulfides and Chemodifferentiated 1,4-Dicarbonyl Systems

Trost, Barry M.,Ornstein, Paul L.

, p. 748 - 751 (2007/10/02)

The use of (E)-2-(hydroxymethyl)cyclopropyl phenyl sulfide as a useful conjunctive reagent, particularly in a stereocontrolled synthesis of vinyl sulfides, is reported.

A CHEMOSELECTIVE DESULFURIZATION METHOD VIA HOMOGENEOUS NICKEL CATALYSIS

Trost, Barry M.,Ornstein, Paul L.

, p. 3463 - 3466 (2007/10/02)

Isopropylmagnesium bromide in the presence of bis-(triphenylphosphino)-nickel(II) chloride reduces vinyl sulfides stereospecifically to the corresponding olefins without overreduction - a process which serves as a key step in the synthesis of the sex pheromone of the Douglas fir tussock moth.

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