18105-64-1 Usage
Uses
Used in Organic Synthesis:
TRI-T-BUTOXYCHLOROSILANE is used as a reagent in organic synthesis for its high reactivity and ability to form various silicone-based materials. Its unique properties make it a valuable component in the synthesis of a wide range of organic compounds.
Used in Silicone Production:
TRI-T-BUTOXYCHLOROSILANE serves as a precursor in the production of various silicone-based materials. Its reactivity and ability to form stable siloxane bonds make it an essential component in the manufacturing process of silicones, which are widely used in industries such as electronics, automotive, aerospace, and construction.
Used in Electronic Industry:
In the electronic industry, TRI-T-BUTOXYCHLOROSILANE is used as a precursor for the production of silicone-based materials, which are utilized in various applications such as encapsulation, potting, and sealing of electronic components. These silicone materials provide excellent electrical insulation, thermal stability, and resistance to environmental factors, ensuring the reliability and longevity of electronic devices.
Used in Automotive Industry:
In the automotive industry, TRI-T-BUTOXYCHLOROSILANE is used in the production of silicone-based materials for applications such as gaskets, seals, and adhesives. These materials offer excellent resistance to temperature extremes, chemicals, and weathering, making them ideal for use in automotive components and systems.
Used in Aerospace Industry:
In the aerospace industry, TRI-T-BUTOXYCHLOROSILANE is used as a precursor for the production of silicone-based materials that are employed in the manufacturing of aircraft components, such as seals, gaskets, and insulating materials. These materials provide excellent performance in extreme temperature and pressure conditions, ensuring the safety and reliability of aerospace systems.
Used in Construction Industry:
In the construction industry, TRI-T-BUTOXYCHLOROSILANE is used in the production of silicone-based materials for applications such as sealants, adhesives, and coatings. These materials offer excellent weather resistance, flexibility, and durability, making them suitable for use in various construction projects, including building facades, windows, and roofing systems.
Check Digit Verification of cas no
The CAS Registry Mumber 18105-64-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,0 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18105-64:
(7*1)+(6*8)+(5*1)+(4*0)+(3*5)+(2*6)+(1*4)=91
91 % 10 = 1
So 18105-64-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H27ClO3Si/c1-10(2,3)14-17(13,15-11(4,5)6)16-12(7,8)9/h1-9H3
18105-64-1Relevant academic research and scientific papers
Docherty, Scott R.,Estes, Deven P.,Copéret, Christophe
, (2018)
Trialkoxysilanols, (RO)3SiOH, are useful as ligands in transition-metal complexes because they provide models for silica-supported metal sites or precursors for the thermolytic precursor approach. However, their synthesis is mostly limited to symmetrical ones, where all RO ligands are the same. However, unsymmetrically substituted trialkoxysilanols could offer significant advantages over their symmetrical counterparts by facilitating crystallization of complexes, lowering crystallographic disorder, changing the thermal properties of the complexes made, and making the addition of pendant functional groups possible. Herein, a simple, general synthetic procedure yielding unsymmetrical trialkoxysilanols (RO)2(R′O)SiOH is presented using imidazole as a promoter.
Gompa, Thaige P.,Jiang, Ningxin,Bacsa, John,La Pierre, Henry S.
, p. 16869 - 16872 (2019)
The direct synthesis of neutral, divalent samarium and europium complexes supported by the bulky bis(tris-tert-butoxysilyl)amide (BTTSA) ligand via oxidative transmetallation is reported. Through the use of a copper(i) ligand complex, conventional lanthanide halide starting materials for complex formation are circumvented and the clean formation of divalent complexes is achieved directly from the bulk metal. The structures of the [Ln(BTTSA)2] (Ln = Sm, Eu) complexes are isotypic, presenting divalent lanthanide ions with distorted, six-coordinate geometries.
