1625-88-3 Usage
General Description
Biphenyl-4-yl(trimethyl)silane is a chemical compound composed of a biphenyl group (a hydrocarbon compound consisting of two benzene rings) connected to a trimethylsilyl group (a silicon atom attached to three methyl groups). biphenyl-4-yl(trimethyl)silane is commonly used as a reagent in organic synthesis, particularly in the field of organosilicon chemistry. It is utilized as a precursor for creating various silane-based compounds, which have applications in industries such as pharmaceuticals, electronics, and materials science. Biphenyl-4-yl(trimethyl)silane is valued for its ability to introduce the silane functional group to organic molecules, enabling the modification of their physical and chemical properties. Additionally, this compound is known for its stability and relatively inert nature, making it a useful tool for manipulating organic molecules in a controlled manner.
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 articles and documents
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.
