13368-45-1 Usage
Uses
Used in Polymer and Resin Production:
BIS(DIMETHYLAMINO)METHYLVINYLSILANE is used as a crosslinking agent to enhance the properties of silicone polymers and resins. Its incorporation improves the mechanical strength, thermal stability, and overall performance of the resulting materials, making them suitable for a wide range of applications, including sealants, adhesives, and coatings.
Used in Semiconductor Industry:
In the semiconductor industry, BIS(DIMETHYLAMINO)METHYLVINYLSILANE is employed as a precursor for chemical vapor deposition (CVD) processes. It is utilized to deposit silicon-containing thin films onto various substrates, which are crucial for the fabrication of microelectronic devices, solar cells, and other advanced technologies. The use of BIS(DIMETHYLAMINO)METHYLVINYLSILANE in CVD processes contributes to the development of high-quality, uniform, and conformal thin films, essential for the performance and reliability of semiconductor devices.
Check Digit Verification of cas no
The CAS Registry Mumber 13368-45-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,6 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13368-45:
(7*1)+(6*3)+(5*3)+(4*6)+(3*8)+(2*4)+(1*5)=101
101 % 10 = 1
So 13368-45-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H18N2Si/c1-7-10(6,8(2)3)9(4)5/h7H,1H2,2-6H3
13368-45-1Relevant academic research and scientific papers
Chloraminosilanes II. Preparation and spectroscopic studies on alkyl-(dimethylamino)chlorosilanes
Washburne,Peterson Jr.
, p. 59 - 64 (2007/10/12)
Several new compounds containing both chloro and dimethylamino groups linked to silicon have been prepared. The general method involved reacting a solution of the appropriate polychlorosilane in ether at ca. - 50° with a chilled ethereal solution of dimethylamine. Prepared in this fashion were CH3Si(NMe2)Cl2, CH3Si(NMe2)2-Cl, PhSi(NMe2)Cl2, PhSi(NMe2)2Cl, CH3(H)Si(NMe2)Cl, (CH3)2Si(NMe2)Cl, CH2CH(CH3)Si(NMe2)Cl, and Ph2Si(NMe2)Cl. Comparison of the spectra of these compounds with those in the perhalo and peramine series showed that replacement of NMe2 for Cl resulted in an upfield shift of the resonances of the other groups linked to silicon, a shift which parallels that observed upon substitution of CH3 for Cl. The relationship of ν(SiH) in the IR and δ(SiH) in the NMR spectra was linear.
