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Trimethyl-((Z)-5-p-tolyl-hex-1-enyloxy)-silane is a complex organic compound with the molecular formula C15H24OSi. It is a colorless liquid at room temperature and is characterized by its unique structure, which includes a trimethylsilyl group (SiMe3), a (Z)-5-p-tolyl-hex-1-enyloxy moiety, and a double bond in the (Z)-configuration. Trimethyl-((Z)-5-p-tolyl-hex-1-enyloxy)-silane is primarily used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds and as a protecting group for alcohols. It is also known for its ability to stabilize certain reactive intermediates in chemical reactions. Due to its reactivity and potential applications in the synthesis of pharmaceuticals and other specialty chemicals, it is an important compound in the field of organic chemistry.

78518-94-2

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78518-94-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78518-94-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,1 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78518-94:
(7*7)+(6*8)+(5*5)+(4*1)+(3*8)+(2*9)+(1*4)=172
172 % 10 = 2
So 78518-94-2 is a valid CAS Registry Number.

78518-94-2Downstream Products

78518-94-2Relevant academic research and scientific papers

REACTION OF CHLOROMETHYLCARBENE WITH TRIMETHYLSILYL ENOL ETHERS. SYNTHESIS OF EUCARVONE, (+/-)-NUCIFERAL AND (+/-)-MANICONE.

Blanco, L.,Slougui, N.,Rousseau, G.,Conia, J. M.

, p. 645 - 648 (2007/10/02)

New synthesis of Eucarvone 7, (+/-)-Nuciferal 12 and (+/-)-Manicone 16 are described from trimethylsilyl enol ethers 2, 10 and 14 via their chloromethylenation products by means of a two carbons homologation reaction.

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