210362-76-8 Usage
Uses
Used in Organic Synthesis:
TRIPHENYL STANNYL DIMETHYL PHENYL SILANE is used as a reagent for introducing a trimethylsilyl group to organic compounds. This modification can enhance the stability, reactivity, or solubility of the target molecules, facilitating various chemical reactions and transformations.
Used in the Synthesis of Organotin and Organosilicon Compounds:
TRIPHENYL STANNYL DIMETHYL PHENYL SILANE serves as a precursor for the synthesis of other organotin and organosilicon compounds. These compounds have diverse applications in various fields, such as pharmaceuticals, materials science, and agrochemicals, due to their unique properties and reactivity.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, TRIPHENYL STANNYL DIMETHYL PHENYL SILANE is used as a key intermediate in the synthesis of bioactive organotin compounds. These compounds exhibit a range of biological activities, including antimicrobial, antiviral, and anticancer properties, making them valuable for the development of new drugs and therapeutic agents.
Used in Materials Science:
In materials science, TRIPHENYL STANNYL DIMETHYL PHENYL SILANE is utilized in the development of organotin-containing polymers and materials with unique properties, such as thermal stability, flame retardancy, and self-healing capabilities. These materials find applications in various industries, including electronics, aerospace, and automotive.
Used in Agrochemical Industry:
In the agrochemical industry, TRIPHENYL STANNYL DIMETHYL PHENYL SILANE is employed in the synthesis of organotin-based pesticides and fungicides. These compounds exhibit potent biocidal activities against various pests and pathogens, contributing to improved crop protection and yield.
Check Digit Verification of cas no
The CAS Registry Mumber 210362-76-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,3,6 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 210362-76:
(8*2)+(7*1)+(6*0)+(5*3)+(4*6)+(3*2)+(2*7)+(1*6)=88
88 % 10 = 8
So 210362-76-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H11Si.3C6H5.Sn/c1-9(2)8-6-4-3-5-7-8;3*1-2-4-6-5-3-1;/h3-7H,1-2H3;3*1-5H;/rC26H26SiSn/c1-27(2,23-15-7-3-8-16-23)28(24-17-9-4-10-18-24,25-19-11-5-12-20-25)26-21-13-6-14-22-26/h3-22H,1-2H3
210362-76-8Relevant academic research and scientific papers
Synthesis and reactivity of stannyloligosilanes, I. Stannyloligosilane chains containing SiMe2 moieties
Uhlig, Frank,Kayser, Christian,Klassen, Ralph,Hermann, Uwe,Brecker, Lothar,Schürmann, Markus,Ruhland-Senge, Karin,Englich, Ulrich
, p. 278 - 287 (2007/10/03)
Stannyloligosilanes 1 and 2 with terminal organotin groups are available by reacting alkali metal tri-or diorganostannides with α,ω-dichloro-or difluorosilanes, or by treatment of organochlorostannanes with α,ω-difluorosilanes in the presence of magnesium. Attempts to functionalize the triorganotin derivatives 2 by halogenation reagents did not result in the halogen compounds 5; instead cleavage of silicon-tin bonds is observed. In contrast, reactions of the hydridotin derivatives 1 with CHX3 (X = Cl, Br) lead to the quantitative formation of the bis(chloro-or bromostannyl)oligosilanes 5. All compounds were characterized by NMR, IR, MS and elemental analysis. In addition, the triorganotin compound 2i and the hydridotin species 1b have been characterized by X-ray crystallography.
A convenient one-pot synthesis of stannylsilanes
Hummeltenberg, Reinhard,Jurkschat, Klaus,Uhlig, Frank
, p. 255 - 261 (2007/10/03)
Stannylsilanes were synthesized in high yields by reaction of organotinchlorides with organofluorosilanes and magnesium. The fluorosilanes were prepared in good yields and under mild conditions by reaction of the corresponding chlorosilanes with [n-Bu4N][Ph3SnF2]. All products were characterized by 29Si, 119Sn NMR spectroscopy and elemental analysis.
