4840-75-9 Usage
Uses
Used in Electronics Industry:
TRIS(DIMETHYLAMINO)PHENYLSILANE is used as a precursor for the synthesis of silicon-based materials for its role in creating stable and uniform thin films, which are essential in electronic components and devices.
Used in Optics Industry:
In the optics field, TRIS(DIMETHYLAMINO)PHENYLSILANE is utilized as a component in the development of materials for optical applications, taking advantage of its ability to form thin films with specific properties required for light transmission and manipulation.
Used in Surface Coating Industry:
TRIS(DIMETHYLAMINO)PHENYLSILANE is employed as a key component in the formulation of surface coatings, where its reactivity and film-forming properties contribute to the creation of durable and high-quality coatings for various substrates.
Used in Materials Chemistry Research:
As a highly reactive organosilicon compound, TRIS(DIMETHYLAMINO)PHENYLSILANE is used as a research chemical for exploring new reactions and developing novel silicon-containing materials with potential applications in various industries.
Used in Ceramics Industry:
In the ceramics sector, TRIS(DIMETHYLAMINO)PHENYLSILANE serves as a precursor for synthesizing silicon-based ceramics, which may exhibit unique mechanical, thermal, and electrical properties beneficial for high-performance applications.
Check Digit Verification of cas no
The CAS Registry Mumber 4840-75-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,4 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4840-75:
(6*4)+(5*8)+(4*4)+(3*0)+(2*7)+(1*5)=99
99 % 10 = 9
So 4840-75-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H23N3Si/c1-13(2)16(14(3)4,15(5)6)12-10-8-7-9-11-12/h7-11H,1-6H3
4840-75-9Relevant 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.
