1027-62-9 Usage
Uses
Used in Chemical Synthesis:
BIS(DIMETHYLAMINO)DIPHENYLSILANE is used as a precursor for the preparation of other chemicals, facilitating the synthesis of various compounds in the chemical industry.
Used in Semiconductor Industry:
In the semiconductor industry, BIS(DIMETHYLAMINO)DIPHENYLSILANE is employed as a reagent to create specific chemical reactions, contributing to the development and manufacturing of semiconductor devices.
Used in Research and Development:
BIS(DIMETHYLAMINO)DIPHENYLSILANE is utilized in research and development settings to explore its potential applications and reactions, further expanding its use in various scientific and industrial fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1027-62-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1027-62:
(6*1)+(5*0)+(4*2)+(3*7)+(2*6)+(1*2)=49
49 % 10 = 9
So 1027-62-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H22N2Si/c1-17(2)19(18(3)4,15-11-7-5-8-12-15)16-13-9-6-10-14-16/h5-14H,1-4H3
1027-62-9Relevant 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.
