18402-22-7 Usage
Uses
Used in Coatings Industry:
N-Tetradecyltrichlorosilane is used as a surface modifier to enhance the hydrophobic and oleophobic properties of coatings, improving their durability and resistance to environmental factors.
Used in Adhesives and Sealants Industry:
In adhesives and sealants, N-Tetradecyltrichlorosilane functions as a surface modifying agent, providing improved adhesion and sealing properties by altering the surface characteristics of the materials to which they are applied.
Used in Polymer and Composites Production:
N-Tetradecyltrichlorosilane is utilized as a component in the manufacturing of polymers and composites, where it contributes to the modification of surface properties, thereby enhancing the overall performance and applicability of the end products.
Used in Optical Films Manufacturing:
N-TETRADECYLTRICHLOROSILANE is employed in the production of optical films, where its surface modifying capabilities are critical for achieving the desired optical properties and performance of the films.
Used in Electronic Materials Industry:
N-Tetradecyltrichlorosilane is used as a surface modifier in the manufacturing of electronic materials, where its ability to alter surface properties can improve the performance and reliability of electronic components and devices.
Check Digit Verification of cas no
The CAS Registry Mumber 18402-22-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,0 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18402-22:
(7*1)+(6*8)+(5*4)+(4*0)+(3*2)+(2*2)+(1*2)=87
87 % 10 = 7
So 18402-22-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H29Cl3Si/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-18(15,16)17/h2-14H2,1H3
18402-22-7Relevant academic research and scientific papers
Contra-thermodynamic Olefin Isomerization by Chain-Walking Hydrofunctionalization and Formal Retro-hydrofunctionalization
Hanna, Steven,Butcher, Trevor W.,Hartwig, John F.
supporting information, p. 7129 - 7133 (2019/09/12)
We report a contra-thermodynamic isomerization of internal olefins to terminal olefins driven by redox reactions and formation of Si-F bonds. This process involves chain-walking hydrosilylation of internal olefins and subsequent formal retro-hydrosilylation. The process rests upon the high activities of platinum hydrosilylation catalysts for isomerization of metal alkyl intermediates and a new, metal-free process for the conversion of alkylsilanes to alkenes. By this approach, 1,2-disubstituted and trisubstituted olefins are converted to terminal olefins.
Synthesis and characterization of biophilic siliconorganic compounds
Aisa, A. M. A.,Kraetzer, D.,Richter, H.
, p. 751 - 758 (2007/10/03)
By biophilic compounds we understand derivatives of sugar or phosphoric acid, starting from mono-, di- or trisilanols with long hydrocarbon chains.Through variation of the lipophilic part (length of the chains, number of the chains) and of the hydrophilic zone (headgroups: OH, OMe, phosphates) the amphiphilic property of our manufactured siliconorganic compounds can be adjusted.With this property, the requirement is given for the formation of vesicles.Beside those diacyloxysilanes already prepared and described by us, new and not yet described siliconorganic compounds could be prepared and characterized.These include the silanols 2a-2c and the methoxy compounds 3a-3c.The silanols 2a-2c should serve as aglyca for the transformation to the silicon sugars.
