1450-22-2 Usage
Uses
Used in Organosilicon Chemistry:
1-Methyl-1,1,2,2,2-pentaphenyldisilane is utilized as a key component in organosilicon chemistry for its ability to form stable silicon-carbon bonds, which is crucial for the synthesis of various organosilicon compounds.
Used in Silicon-Based Materials and Devices:
In the field of materials science, 1-Methyl-1,1,2,2,2-pentaphenyldisilane is employed as a precursor for developing silicon-based materials, which are essential in a range of applications due to their unique electronic, mechanical, and thermal properties.
Used in Electronic and Optoelectronic Applications:
1-Methyl-1,1,2,2,2-pentaphenyldisilane is used as a material in electronic and optoelectronic applications due to its potential to enhance the performance of devices such as transistors, solar cells, and light-emitting diodes (LEDs), leveraging its electronic properties.
Used in Chemical Vapor Deposition Processes:
As a precursor in chemical vapor deposition (CVD) processes, 1-Methyl-1,1,2,2,2-pentaphenyldisilane is instrumental in the production of silicon-based thin films. These films are vital for various applications, including semiconductor devices, sensors, and coatings, due to their controlled thickness and uniformity.
Check Digit Verification of cas no
The CAS Registry Mumber 1450-22-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,5 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1450-22:
(6*1)+(5*4)+(4*5)+(3*0)+(2*2)+(1*2)=52
52 % 10 = 2
So 1450-22-2 is a valid CAS Registry Number.
1450-22-2Relevant academic research and scientific papers
Preparation of New Monomeric, Oligomeric, and Polymeric Silyl Triflates
Uhlig, Wolfram
, p. 47 - 54 (2007/10/02)
The highly reactive silyl triflates R3SiOSO2CF3 are valuable reagents in organosilicon chemistry.New triflate derivatives of mono- and oligosilanes have been prepared by substitution of phenyl groups or hydrogen atoms for the trifluoromethanesulfonyl group.The presence of the electron-withdrawing triflate group leads to a strong deactivation of the other substituents at the silicon atom, and the displacement of a second phenyl group at the same silicon atom is much slower than the first step.For this reason in the case of phenylated oligosilanes stepwisemonosubstitution of the silicon atoms has been found.Other new oligomeric silyl triflates are obtained by reaction of silanediyl(triyl) bis(tris)(trifluoromethanesulfonates) with lithium derivatives of organosilicon compounds.Finally, the cleavage of silicon - phenyl bonds of poly by CF3SO3H leads to triflate derivatives of polysilanes. Key Words: Silyl triflates / Organosilanes
