2003-92-1

Usage

Uses

Used in Chemical Synthesis:
1,1,1,3,5,7,7,7-OCTAMETHYL-3,5-BIS(TRIM& is utilized as an organic synthetic intermediate, playing a crucial role in the synthesis of various complex organic molecules. Its unique structure and properties facilitate the formation of new chemical bonds and the creation of novel compounds.
Used in Chemical Reactions:
As a reagent, 1,1,1,3,5,7,7,7-OCTAMETHYL-3,5-BIS(TRIM& is employed in a wide range of chemical reactions. Its high thermal stability and inertness make it a reliable component in processes that require controlled conditions and precise outcomes.
Used in the Chemical Industry:
1,1,1,3,5,7,7,7-OCTAMETHYL-3,5-BIS(TRIM& is also used in various applications within the chemical industry, where its properties of thermal stability and inertness are highly valued. This includes its use in the production of specialty chemicals, materials, and other industrial products that require specific performance characteristics.

InChI:InChI=1/C14H42O5Si6/c1-20(2,3)15-24(13,16-21(4,5)6)19-25(14,17-22(7,8)9)18-23(10,11)12/h1-14H3

Upstream product

• 75-77-4 chloro-trimethyl-silane 
• 75-79-6 Methyltrichlorosilane 
• 1873-88-7 1,1,1,3,5,5,5-heptamethyltrisiloxan 
• 100-53-8 phenylmethanethiol 
• 6493-73-8 dibenzyltrisulfide 

Relevant academic research and scientific papers

Silylating Disulfides and Thiols with Hydrosilicones Catalyzed by B(C6F5)3

Hydrosilanes and silicones, catalyzed with B(C6F5)3, may be used to silylate thiols or cleave disulfides giving silyl thio ethers. Alcohols were found to react faster than thiols or disulfides, while alkoxysilanes (the Piers-Rubinsztajn reaction) were slower such that the overall order of reactivity was found to be HO>HS>SS>SiOEt. The resulting silane and silicone-protected thio ethers produced from the sulfur-based functional groups could be cleaved to thiols using alcohols or mild acid with rates that depend on the steric bulk of the siloxane.

MUTUAL EFFECT OF SOLUTIONS OF SALTS AND HCl ON COHYDROLYSIS OF METHYLCHLOROSILANES

In hydrolytic polycondensation of Me2SiCl2, the combined effect of salts and HCl causes a decrease in the yield of 4, and this effect increases with an increase in the binding strength of the water with the salt in hydrate complexes and the concentration of HCl.The combined effect of salts and HCl on the composition of the products of the reaction in hydrolytic copolycondensation of Me2SiCl2 with Me3SiCl and MeSiCl3 with Me3SiCl increases with an increase in the degree of binding of water in hydrate complexes, caused by competition in the formation of hydrate complexes between the salt and HCl.