210362-73-5 Usage
Uses
Used in Organic Synthesis:
TRIPHENYL STANNYL DIMETHYL VINYL SILANE is utilized as a reagent for the preparation of vinylated organotin compounds, which are important in the synthesis of various organic molecules and materials. Its ability to facilitate the formation of vinyl groups on organotin compounds makes it a valuable component in this process.
Used in Cross-Coupling Reactions:
In the field of organic chemistry, TRIPHENYL STANNYL DIMETHYL VINYL SILANE serves as a cross-coupling reagent, which is instrumental in the construction of carbon-carbon bonds. This role is crucial for the synthesis of complex organic molecules and contributes to the advancement of chemical research and development.
Used in Chemical Research:
TRIPHENYL STANNYL DIMETHYL VINYL SILANE is also employed in academic and industrial research settings to explore new methods and pathways in chemical reactions. Its unique properties allow researchers to investigate novel approaches to bond formation and molecular assembly.
Used in Environmentally Conscious Applications:
Given the compound's potential environmental impact, it is used in applications that prioritize green chemistry and sustainable practices. This includes the development of processes that minimize waste, reduce toxicity, and promote the efficient use of resources in chemical production.
Check Digit Verification of cas no
The CAS Registry Mumber 210362-73-5 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 210362-73:
(8*2)+(7*1)+(6*0)+(5*3)+(4*6)+(3*2)+(2*7)+(1*3)=85
85 % 10 = 5
So 210362-73-5 is a valid CAS Registry Number.
InChI:InChI=1/3C6H5.C4H9Si.Sn/c3*1-2-4-6-5-3-1;1-4-5(2)3;/h3*1-5H;4H,1H2,2-3H3;/rC22H24SiSn/c1-4-23(2,3)24(20-14-8-5-9-15-20,21-16-10-6-11-17-21)22-18-12-7-13-19-22/h4-19H,1H2,2-3H3
210362-73-5Relevant academic research and scientific papers
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.
