69397-47-3

Usage

Uses

Used in Organic Synthesis:
(2,2-Dimethyl-propionyl)-tris(trimethylsilyl)silane is used as a reagent for the protection of alcohols and carboxylic acids in organic synthesis. This protection allows for selective reactions to occur at other sites on a molecule without affecting the protected functional groups.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (2,2-Dimethyl-propionyl)-tris(trimethylsilyl)silane is utilized in the synthesis of various drugs. Its ability to protect certain functional groups simplifies the synthesis process and can lead to the production of complex molecules with greater ease.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, this silane derivative is employed for the synthesis of various agrochemicals. Its protective properties aid in the creation of molecules with specific reactivity, which is crucial for the development of effective agricultural products.
Used in Semiconductor Industry:
(2,2-Dimethyl-propionyl)-tris(trimethylsilyl)silane also finds application in the semiconductor industry as a surface modifier for silicon substrates. This modification can enhance the properties of the substrate, improving the performance of semiconductor devices.

Upstream product

• 3282-30-2 pivaloyl chloride 
• 4098-98-0 tetrakis(trimethylsilyl)silane 
• 1873-77-4 tris-(trimethylsilyl)silane 
• 4110-02-5 tris(trimethylsilyl)silyllithium 

Downstream Products

• 69397-61-1 C₁₇H₃₄O₂Si₃ 
• 69397-60-0 C₂₀H₄₂O₂Si₄ 

Relevant academic research and scientific papers

Stable Solid Silaethylenes

A solid silaethylene, 1,1-bis(trimethylsilyl)-2-(trimethylsiloxy)-1-(1-adamantyl)-1-silaethene (2c), has been isolated from the photolysis of the isomeric acylsilane.The silaethylene was characterized by IR, Raman, UV, 1H NMR, 13C NMR, 29Si NMR, and mass spectroscopy and by its ionization potential.The crystal structure shows a slightly twisted molecule with a silicn-carbon double-bond length of 1.764 Angstroem.The molecule smokes vigorously in air, yielding a cyclic trisiloxane and the silyl ester of adamantane-1-carboxylic acid.Other reactions and comparisons with other silaethylenes in solution are described.In addition, 1,1-bis(trimethylsilyl)-2-(trimethylsiloxy)-2-(1,1-diethylpropyl)-1-silaethene (2b) has been obtained as a solid.

Silenes as novel synthetic reagents: Identification of a practical method for silene generation and trapping

The elucidation of a robust and reliable sequence for the generation of highly reactive transient silenes from simple aldehydes is described. The key step involves a silyl-modified Peterson olefination which critically depends on the presence of a sub-sto

A new and easy route to polysilanylpotassium compounds

A method is presented for the synthesis of tertiary, secondary, and primary polysilylpotassium compounds. Reaction of potassium tert-butoxide, in either DME or THF, with a suitable precursor molecule, proceeds by cleavage of a trimethylsilyl - polysilanyl bond, and formation of trimethylsilyl tert-butyl ether and a polysilanylpotassium compound. This route allows easy and flexible access to a number of novel polysilanylpotassium compounds, avoiding the hitherto common use of poisonous mercury compounds.