332343-84-7 Usage
Description
Bis(2-methoxyphenyl)-1,1,2,2-tetramethyldisilane, 95% is an organosilane compound characterized by its two methoxyphenyl groups and a tetramethyldisilane backbone. It is a versatile reagent in organic synthesis, known for its ability to form stable C-Si bonds.
Uses
Used in Organic Synthesis:
Bis(2-methoxyphenyl)-1,1,2,2-tetramethyldisilane, 95% is used as a reagent for the installation of C-Si bonds in organic molecules. The C-Si bond formed is easily cleaved by Tamao-Fleming oxidation, making it a valuable tool in the synthesis of various organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Bis(2-methoxyphenyl)-1,1,2,2-tetramethyldisilane, 95% is used as a precursor for the synthesis of bioactive compounds. The C-Si bond can be selectively cleaved to release the desired product, providing a controlled and efficient synthetic route.
Used in Material Science:
In material science, Bis(2-methoxyphenyl)-1,1,2,2-tetramethyldisilane, 95% is used in the development of new materials with unique properties. The C-Si bond can be incorporated into polymers and other materials to enhance their stability, reactivity, or other characteristics.
Used in Nanotechnology:
In nanotechnology, Bis(2-methoxyphenyl)-1,1,2,2-tetramethyldisilane, 95% is used in the synthesis of nanoparticles and other nanostructures. The C-Si bond can be used to control the size, shape, and properties of these nanostructures, enabling their use in various applications such as drug delivery, catalysis, and electronics.
Check Digit Verification of cas no
The CAS Registry Mumber 332343-84-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,2,3,4 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 332343-84:
(8*3)+(7*3)+(6*2)+(5*3)+(4*4)+(3*3)+(2*8)+(1*4)=117
117 % 10 = 7
So 332343-84-7 is a valid CAS Registry Number.
InChI:InChI=1/C18H26O2Si2/c1-19-15-11-7-9-13-17(15)21(3,4)22(5,6)18-14-10-8-12-16(18)20-2/h7-14H,1-6H3
332343-84-7Relevant articles and documents
(2-methoxyphenyl)dimethylsilyl lithium and cuprate reagents offer unique advantages in multistep synthesis
Lee, Thomas W.,Corey
, p. 3337 - 3339 (2007/10/03)
Equation presented The new silyllithium reagent 1 and the corresponding cyanocuprate 3 are readily generated under optimal conditions and are useful for the formation of C-Si bonds. Tamao-Fleming oxidation of such C-Si bonds can be effected under very mild conditions.