1625-88-3 Usage
Uses
Used in Organic Synthesis:
Biphenyl-4-yl(trimethyl)silane is used as a reagent in organic synthesis, particularly in the field of organosilicon chemistry. It serves as a precursor for creating various silane-based compounds, which have applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, biphenyl-4-yl(trimethyl)silane is used as a precursor for the synthesis of silane-based compounds that can be incorporated into drug molecules. The introduction of the silane functional group can modify the physical and chemical properties of these molecules, potentially enhancing their therapeutic effects.
Used in Electronics Industry:
Biphenyl-4-yl(trimethyl)silane is also utilized in the electronics industry, where silane-based compounds derived from biphenyl-4-yl(trimethyl)silane can be used in the fabrication of electronic devices and components. The modification of organic molecules with silane functional groups can improve the performance and reliability of these devices.
Used in Materials Science:
In materials science, biphenyl-4-yl(trimethyl)silane is used as a precursor for the development of new materials with specific properties. The incorporation of silane functional groups can lead to the creation of materials with improved mechanical, thermal, or electrical properties, depending on the application.
Check Digit Verification of cas no
The CAS Registry Mumber 1625-88-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1625-88:
(6*1)+(5*6)+(4*2)+(3*5)+(2*8)+(1*8)=83
83 % 10 = 3
So 1625-88-3 is a valid CAS Registry Number.
1625-88-3Relevant academic research and scientific papers
Selective aromatic carbon-oxygen bond cleavage of trifluoromethoxyarenes: a trifluoromethoxy group as a convertible directing group
Iijima, Akinori,Amii, Hideki
scheme or table, p. 6013 - 6015 (2009/04/11)
An efficient method for selective activation of aromatic C-O bonds in trifluoromethoxyarenes is developed. Upon treatment with a metallic sodium/chlorotrimethylsilane system, trifluoromethoxyarenes undergo reductive dealkoxylation to provide the corresponding arylsilanes. Also the synthetic applications of the present reactions combined with ortho-metallation are described.
