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1,1,1,3,3,3-Hexaphenyl-2-triphenylsilanyl-trisilane is a complex organosilicon compound characterized by its unique molecular structure. It consists of a central silicon atom bonded to three other silicon atoms, forming a trisilane backbone. Each of these silicon atoms is further connected to phenyl groups, with the central silicon atom having three phenyl groups attached, and the terminal silicon atoms each having one phenyl group. Additionally, one of the terminal silicon atoms is connected to a triphenylsilanyl group, which is a silicon atom bonded to three phenyl groups. 1,1,1,3,3,3-hexaphenyl-2-triphenylsilanyl-trisilane is known for its stability and is often used in the synthesis of other organosilicon compounds due to its ability to act as a precursor. The hexaphenyl-2-triphenylsilanyl-trisilane is a significant molecule in the field of organosilicon chemistry, showcasing the diversity and complexity of silicon-based compounds.

4098-88-8

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4098-88-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4098-88-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,9 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4098-88:
(6*4)+(5*0)+(4*9)+(3*8)+(2*8)+(1*8)=108
108 % 10 = 8
So 4098-88-8 is a valid CAS Registry Number.

4098-88-8Upstream product

4098-88-8Downstream Products

4098-88-8Relevant academic research and scientific papers

Bulky Phenyl Modifications of the Silanide Ligand Si(SiMe3)3 – Synthesis and Reactivity

Schmidt, Patrick,Fietze, Sascha,Schrenk, Claudio,Schnepf, Andreas

, p. 1759 - 1765 (2017)

The synthesis and structural characterization of bulkier variations of the very common organometallic compound MSi(SiMe3)3, namely MSi(SiMe3)(SiPh3)2 3 and MSi(SiPh3)3 [M = Li (1), K (5)] are presented, which can be synthesized via a step by step exchange of SiMe3 groups by bulkier SiPh3 groups. This synthetic route is high selective and is performed in good yields via the silanes Si(SiMe3)2(SiPh3)2 (2) and Si(SiMe3)(SiPh3)3 (4). Additionally, the corresponding silanes HSi(SiMe3)(SiPh3)2 (6H) and HSi(SiPh3)3 (7H) are obtained via the reaction of 3 and 5 with aqueous HCl, respectively. Oxidation of 6H with CCl4 gives the chlorsilane Cl-Si(SiMe3)(SiPh3)2 (6Cl). The bulkiest chlorsilane Cl–Si(SiPh3)3 (7) is obtained by the reaction of 5 with ECl2 (E = Sn, Pb).

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