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Tris(2-phenylethyl)silane is an organosilicon compound with the chemical formula C24H24Si. It is a colorless, crystalline solid that is insoluble in water but soluble in organic solvents. tris(2-phenylethyl)silane is characterized by its three 2-phenylethyl groups attached to a central silicon atom. It is primarily used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds through the Peterson olefination reaction. Tris(2-phenylethyl)silane is also known for its ability to act as a reducing agent in certain chemical transformations. Due to its stability and reactivity, it has found applications in the synthesis of various pharmaceuticals and specialty chemicals.

18751-11-6

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18751-11-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18751-11-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,5 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18751-11:
(7*1)+(6*8)+(5*7)+(4*5)+(3*1)+(2*1)+(1*1)=116
116 % 10 = 6
So 18751-11-6 is a valid CAS Registry Number.

18751-11-6Relevant academic research and scientific papers

Formal SiH4 chemistry using stable and easy-to-handle surrogates

Simonneau, Antoine,Oestreich, Martin

, p. 816 - 822 (2015/10/05)

Monosilane (SiH4) is far less well behaved than its carbon analogue methane (CH4). It is a colourless gas that is industrially relevant as a source of elemental silicon, but its pyrophoric and explosive nature makes its handling and use challenging. Consequently, synthetic applications of SiH4 in academic laboratories are extremely rare and methodologies based on SiH4 are underdeveloped. Safe and controlled alternatives to the substituent redistribution approaches of hydrosilanes are desirable and cyclohexa-2,5-dien-1-ylsilanes where the cyclohexa-1,4-diene units serve as placeholders for the hydrogen atoms have been identified as potent surrogates of SiH4. We disclose here that the commercially available Lewis acid tris(pentafluorophenyl)borane, B(C6F5)3, is able to promote the release of the Si-H bond catalytically while subsequently enabling the hydrosilylation of C-C multiple bonds in the same pot. The net reactions are transition-metal-free transfer hydrosilylations with SiH4 as a building block for the preparation of various hydrosilanes.

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