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2,2,5,5-Tetramethyl-3-phenyl-1,2,5-oxadisilolane is a complex organic compound with the molecular formula C14H22OSi2. It is a derivative of oxadisilolane, which is a type of cyclic siloxane. 2,2,5,5-tetramethyl-3-phenyl-1,2,5-oxadisilolane features a six-membered ring structure with two silicon atoms, two oxygen atoms, and a phenyl group attached to one of the silicon atoms. The molecule also has four methyl groups (CH3) attached to the silicon atoms, which contribute to its stability and reactivity. 2,2,5,5-Tetramethyl-3-phenyl-1,2,5-oxadisilolane is primarily used as a reagent in organic synthesis, particularly in the formation of silicon-containing compounds. Its unique structure allows for various applications in the field of materials science, such as the synthesis of silicone polymers and the development of new materials with specific properties.

3294-30-2

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3294-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3294-30-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,9 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3294-30:
(6*3)+(5*2)+(4*9)+(3*4)+(2*3)+(1*0)=82
82 % 10 = 2
So 3294-30-2 is a valid CAS Registry Number.

3294-30-2Downstream Products

3294-30-2Relevant academic research and scientific papers

An Electroreductive Approach to Radical Silylation via the Activation of Strong Si-Cl Bond

Lu, Lingxiang,Siu, Juno C.,Lai, Yihuan,Lin, Song

, p. 21272 - 21278 (2020/12/21)

The construction of C(sp3)-Si bonds is important in synthetic, medicinal, and materials chemistry. In this context, reactions mediated by silyl radicals have become increasingly attractive but methods for accessing these intermediates remain limited. We present a new strategy for silyl radical generation via electroreduction of readily available chlorosilanes. At highly biased potentials, electrochemistry grants access to silyl radicals through energetically uphill reductive cleavage of strong Si-Cl bonds. This strategy proved to be general in various alkene silylation reactions including disilylation, hydrosilylation, and allylic silylation under simple and transition-metal-free conditions.

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